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Items: 1 to 20 of 6504

1.

rs3088142 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    C>G,T [Show Flanks]
    Chromosome:
    10:75094806 (GRCh38)
    10:76854564 (GRCh37)
    Canonical SPDI:
    NC_000010.11:75094805:C:G,NC_000010.11:75094805:C:T
    Gene:
    DUSP13 (Varview)
    Functional Consequence:
    coding_sequence_variant,genic_downstream_transcript_variant,3_prime_UTR_variant,missense_variant
    Clinical significance:
    benign
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    T=0.447299/165183 (ALFA)
    C=0.082969/152 (Korea1K)
    C=0.0843/247 (KOREAN)
    C=0.087338/1464 (TOMMO)
    C=0.105863/65 (Vietnamese)
    C=0.18595/90 (SGDP_PRJ)
    C=0.25/11 (Siberian)
    T=0.309524/26 (PRJEB36033)
    C=0.317311/24973 (PAGE_STUDY)
    C=0.326271/616 (HapMap)
    C=0.32853/684 (HGDP_Stanford)
    C=0.347222/75 (Qatari)
    T=0.348333/209 (NorthernSweden)
    T=0.35/14 (GENOME_DK)
    C=0.359151/1799 (1000Genomes)
    T=0.404515/1559 (ALSPAC)
    T=0.409655/1519 (TWINSUK)
    T=0.425852/425 (GoNL)
    T=0.439732/1970 (Estonian)
    C=0.445015/117791 (TOPMED)
    T=0.447566/239 (MGP)
    C=0.472658/118483 (GnomAD_exomes)
    C=0.473344/66289 (GnomAD)
    T=0.480132/145 (FINRISK)
    C=0.480922/58004 (ExAC)
    C=0.495156/6440 (GoESP)
    HGVS:
    NC_000010.11:g.75094806C>G, NC_000010.11:g.75094806C>T, NC_000010.10:g.76854564C>G, NC_000010.10:g.76854564C>T, NG_033976.1:g.19407G>C, NG_033976.1:g.19407G>A, NM_016364.3:c.467G>C, NM_016364.3:c.467G>A, NM_001007271.2:c.*775G>C, NM_001007271.2:c.*775G>A, NM_001007271.1:c.*775G>C, NM_001007271.1:c.*775G>A, NM_001320842.2:c.746G>C, NM_001320842.2:c.746G>A, NM_001320842.1:c.746G>C, NM_001320842.1:c.746G>A, NM_001363514.2:c.875G>C, NM_001363514.2:c.875G>A, NM_001363514.1:c.875G>C, NM_001363514.1:c.875G>A, NM_001007273.2:c.746G>C, NM_001007273.2:c.746G>A, NM_001007273.1:c.746G>C, NM_001007273.1:c.746G>A, NM_001320843.2:c.467G>C, NM_001320843.2:c.467G>A, NM_001320843.1:c.467G>C, NM_001320843.1:c.467G>A, NM_001007272.2:c.617G>C, NM_001007272.2:c.617G>A, NM_001007272.1:c.617G>C, NM_001007272.1:c.617G>A, XM_005269883.4:c.1124G>C, XM_005269883.4:c.1124G>A, XM_005269883.3:c.1124G>C, XM_005269883.3:c.1124G>A, XM_005269883.2:c.1124G>C, XM_005269883.2:c.1124G>A, XM_005269883.1:c.1124G>C, XM_005269883.1:c.1124G>A, XM_011539855.3:c.467G>C, XM_011539855.3:c.467G>A, XM_011539855.2:c.467G>C, XM_011539855.2:c.467G>A, XM_011539855.1:c.467G>C, XM_011539855.1:c.467G>A, NM_001007274.1:c.*633G>C, NM_001007274.1:c.*633G>A, NM_001007275.1:c.*529G>C, NM_001007275.1:c.*529G>A, XM_047425305.1:c.467G>C, XM_047425305.1:c.467G>A, XM_047425308.1:c.467G>C, XM_047425308.1:c.467G>A, XM_047425306.1:c.467G>C, XM_047425306.1:c.467G>A, NP_057448.3:p.Cys156Ser, NP_057448.3:p.Cys156Tyr, NP_001307771.1:p.Cys249Ser, NP_001307771.1:p.Cys249Tyr, NP_001350443.1:p.Cys292Ser, NP_001350443.1:p.Cys292Tyr, NP_001007274.1:p.Cys249Ser, NP_001007274.1:p.Cys249Tyr, NP_001307772.1:p.Cys156Ser, NP_001307772.1:p.Cys156Tyr, NP_001007273.1:p.Cys206Ser, NP_001007273.1:p.Cys206Tyr, XP_005269940.1:p.Cys375Ser, XP_005269940.1:p.Cys375Tyr, XP_011538157.1:p.Cys156Ser, XP_011538157.1:p.Cys156Tyr, XP_047281261.1:p.Cys156Ser, XP_047281261.1:p.Cys156Tyr, XP_047281264.1:p.Cys156Ser, XP_047281264.1:p.Cys156Tyr, XP_047281262.1:p.Cys156Ser, XP_047281262.1:p.Cys156Tyr

    PubMedLitVar

    2.

    rs16931996 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      G>A,C [Show Flanks]
      Chromosome:
      10:75094705 (GRCh38)
      10:76854463 (GRCh37)
      Canonical SPDI:
      NC_000010.11:75094704:G:A,NC_000010.11:75094704:G:C
      Gene:
      DUSP13 (Varview)
      Functional Consequence:
      genic_downstream_transcript_variant,coding_sequence_variant,stop_gained,missense_variant,3_prime_UTR_variant
      Clinical significance:
      benign
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      C=0.002456/270 (ALFA)
      C=0.000259/1 (ALSPAC)
      C=0.000539/2 (TWINSUK)
      C=0.001002/1 (GoNL)
      C=0.001263/1 (PRJEB37584)
      C=0.001873/1 (MGP)
      C=0.030762/154 (1000Genomes)
      C=0.031897/4472 (GnomAD)
      C=0.033688/8917 (TOPMED)
      C=0.035753/465 (GoESP)
      C=0.037037/8 (Qatari)
      C=0.042424/14 (HapMap)
      G=0.5/12 (SGDP_PRJ)
      HGVS:
      NC_000010.11:g.75094705G>A, NC_000010.11:g.75094705G>C, NC_000010.10:g.76854463G>A, NC_000010.10:g.76854463G>C, NG_033976.1:g.19508C>T, NG_033976.1:g.19508C>G, NM_016364.3:c.568C>T, NM_016364.3:c.568C>G, NM_001007271.2:c.*876C>T, NM_001007271.2:c.*876C>G, NM_001007271.1:c.*876C>T, NM_001007271.1:c.*876C>G, NM_001320842.2:c.847C>T, NM_001320842.2:c.847C>G, NM_001320842.1:c.847C>T, NM_001320842.1:c.847C>G, NM_001363514.2:c.976C>T, NM_001363514.2:c.976C>G, NM_001363514.1:c.976C>T, NM_001363514.1:c.976C>G, NM_001007273.2:c.847C>T, NM_001007273.2:c.847C>G, NM_001007273.1:c.847C>T, NM_001007273.1:c.847C>G, NM_001320843.2:c.568C>T, NM_001320843.2:c.568C>G, NM_001320843.1:c.568C>T, NM_001320843.1:c.568C>G, NM_001007272.2:c.718C>T, NM_001007272.2:c.718C>G, NM_001007272.1:c.718C>T, NM_001007272.1:c.718C>G, XM_005269883.4:c.1225C>T, XM_005269883.4:c.1225C>G, XM_005269883.3:c.1225C>T, XM_005269883.3:c.1225C>G, XM_005269883.2:c.1225C>T, XM_005269883.2:c.1225C>G, XM_005269883.1:c.1225C>T, XM_005269883.1:c.1225C>G, XM_011539855.3:c.568C>T, XM_011539855.3:c.568C>G, XM_011539855.2:c.568C>T, XM_011539855.2:c.568C>G, XM_011539855.1:c.568C>T, XM_011539855.1:c.568C>G, NM_001007274.1:c.*734C>T, NM_001007274.1:c.*734C>G, NM_001007275.1:c.*630C>T, NM_001007275.1:c.*630C>G, XM_047425305.1:c.568C>T, XM_047425305.1:c.568C>G, XM_047425308.1:c.568C>T, XM_047425308.1:c.568C>G, XM_047425306.1:c.568C>T, XM_047425306.1:c.568C>G, NP_057448.3:p.Arg190Ter, NP_057448.3:p.Arg190Gly, NP_001307771.1:p.Arg283Ter, NP_001307771.1:p.Arg283Gly, NP_001350443.1:p.Arg326Ter, NP_001350443.1:p.Arg326Gly, NP_001007274.1:p.Arg283Ter, NP_001007274.1:p.Arg283Gly, NP_001307772.1:p.Arg190Ter, NP_001307772.1:p.Arg190Gly, NP_001007273.1:p.Arg240Ter, NP_001007273.1:p.Arg240Gly, XP_005269940.1:p.Arg409Ter, XP_005269940.1:p.Arg409Gly, XP_011538157.1:p.Arg190Ter, XP_011538157.1:p.Arg190Gly, XP_047281261.1:p.Arg190Ter, XP_047281261.1:p.Arg190Gly, XP_047281264.1:p.Arg190Ter, XP_047281264.1:p.Arg190Gly, XP_047281262.1:p.Arg190Ter, XP_047281262.1:p.Arg190Gly

      3.

      rs61737441 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        C>A,G,T [Show Flanks]
        Chromosome:
        10:75094704 (GRCh38)
        10:76854462 (GRCh37)
        Canonical SPDI:
        NC_000010.11:75094703:C:A,NC_000010.11:75094703:C:G,NC_000010.11:75094703:C:T
        Gene:
        DUSP13 (Varview)
        Functional Consequence:
        missense_variant,3_prime_UTR_variant,genic_downstream_transcript_variant,coding_sequence_variant
        Clinical significance:
        benign
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        T=0.000202/39 (ALFA)
        T=0.000035/1 (TOMMO)
        T=0.003998/52 (GoESP)
        T=0.004841/24 (1000Genomes)
        T=0.005808/457 (PAGE_STUDY)
        C=0.5/3 (SGDP_PRJ)
        HGVS:
        NC_000010.11:g.75094704C>A, NC_000010.11:g.75094704C>G, NC_000010.11:g.75094704C>T, NC_000010.10:g.76854462C>A, NC_000010.10:g.76854462C>G, NC_000010.10:g.76854462C>T, NG_033976.1:g.19509G>T, NG_033976.1:g.19509G>C, NG_033976.1:g.19509G>A, NM_016364.3:c.569G>T, NM_016364.3:c.569G>C, NM_016364.3:c.569G>A, NM_001007271.2:c.*877G>T, NM_001007271.2:c.*877G>C, NM_001007271.2:c.*877G>A, NM_001007271.1:c.*877G>T, NM_001007271.1:c.*877G>C, NM_001007271.1:c.*877G>A, NM_001320842.2:c.848G>T, NM_001320842.2:c.848G>C, NM_001320842.2:c.848G>A, NM_001320842.1:c.848G>T, NM_001320842.1:c.848G>C, NM_001320842.1:c.848G>A, NM_001363514.2:c.977G>T, NM_001363514.2:c.977G>C, NM_001363514.2:c.977G>A, NM_001363514.1:c.977G>T, NM_001363514.1:c.977G>C, NM_001363514.1:c.977G>A, NM_001007273.2:c.848G>T, NM_001007273.2:c.848G>C, NM_001007273.2:c.848G>A, NM_001007273.1:c.848G>T, NM_001007273.1:c.848G>C, NM_001007273.1:c.848G>A, NM_001320843.2:c.569G>T, NM_001320843.2:c.569G>C, NM_001320843.2:c.569G>A, NM_001320843.1:c.569G>T, NM_001320843.1:c.569G>C, NM_001320843.1:c.569G>A, NM_001007272.2:c.719G>T, NM_001007272.2:c.719G>C, NM_001007272.2:c.719G>A, NM_001007272.1:c.719G>T, NM_001007272.1:c.719G>C, NM_001007272.1:c.719G>A, XM_005269883.4:c.1226G>T, XM_005269883.4:c.1226G>C, XM_005269883.4:c.1226G>A, XM_005269883.3:c.1226G>T, XM_005269883.3:c.1226G>C, XM_005269883.3:c.1226G>A, XM_005269883.2:c.1226G>T, XM_005269883.2:c.1226G>C, XM_005269883.2:c.1226G>A, XM_005269883.1:c.1226G>T, XM_005269883.1:c.1226G>C, XM_005269883.1:c.1226G>A, XM_011539855.3:c.569G>T, XM_011539855.3:c.569G>C, XM_011539855.3:c.569G>A, XM_011539855.2:c.569G>T, XM_011539855.2:c.569G>C, XM_011539855.2:c.569G>A, XM_011539855.1:c.569G>T, XM_011539855.1:c.569G>C, XM_011539855.1:c.569G>A, NM_001007274.1:c.*735G>T, NM_001007274.1:c.*735G>C, NM_001007274.1:c.*735G>A, NM_001007275.1:c.*631G>T, NM_001007275.1:c.*631G>C, NM_001007275.1:c.*631G>A, XM_047425305.1:c.569G>T, XM_047425305.1:c.569G>C, XM_047425305.1:c.569G>A, XM_047425308.1:c.569G>T, XM_047425308.1:c.569G>C, XM_047425308.1:c.569G>A, XM_047425306.1:c.569G>T, XM_047425306.1:c.569G>C, XM_047425306.1:c.569G>A, NP_057448.3:p.Arg190Leu, NP_057448.3:p.Arg190Pro, NP_057448.3:p.Arg190Gln, NP_001307771.1:p.Arg283Leu, NP_001307771.1:p.Arg283Pro, NP_001307771.1:p.Arg283Gln, NP_001350443.1:p.Arg326Leu, NP_001350443.1:p.Arg326Pro, NP_001350443.1:p.Arg326Gln, NP_001007274.1:p.Arg283Leu, NP_001007274.1:p.Arg283Pro, NP_001007274.1:p.Arg283Gln, NP_001307772.1:p.Arg190Leu, NP_001307772.1:p.Arg190Pro, NP_001307772.1:p.Arg190Gln, NP_001007273.1:p.Arg240Leu, NP_001007273.1:p.Arg240Pro, NP_001007273.1:p.Arg240Gln, XP_005269940.1:p.Arg409Leu, XP_005269940.1:p.Arg409Pro, XP_005269940.1:p.Arg409Gln, XP_011538157.1:p.Arg190Leu, XP_011538157.1:p.Arg190Pro, XP_011538157.1:p.Arg190Gln, XP_047281261.1:p.Arg190Leu, XP_047281261.1:p.Arg190Pro, XP_047281261.1:p.Arg190Gln, XP_047281264.1:p.Arg190Leu, XP_047281264.1:p.Arg190Pro, XP_047281264.1:p.Arg190Gln, XP_047281262.1:p.Arg190Leu, XP_047281262.1:p.Arg190Pro, XP_047281262.1:p.Arg190Gln

        4.

        rs79802987 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          G>A,T [Show Flanks]
          Chromosome:
          10:75103934 (GRCh38)
          10:76863692 (GRCh37)
          Canonical SPDI:
          NC_000010.11:75103933:G:A,NC_000010.11:75103933:G:T
          Gene:
          DUSP13 (Varview), SAMD8 (Varview)
          Functional Consequence:
          coding_sequence_variant,missense_variant,3_prime_UTR_variant,genic_upstream_transcript_variant,intron_variant
          Clinical significance:
          benign
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          A=0.001917/153 (ALFA)
          A=0.007185/167 (ExAC)
          A=0.010673/138 (GoESP)
          A=0.011349/3004 (TOPMED)
          A=0.012336/62 (1000Genomes)
          G=0.5/3 (SGDP_PRJ)
          HGVS:
          NC_000010.11:g.75103934G>A, NC_000010.11:g.75103934G>T, NC_000010.10:g.76863692G>A, NC_000010.10:g.76863692G>T, NG_033976.1:g.10279C>T, NG_033976.1:g.10279C>A, NM_001007271.2:c.*172C>T, NM_001007271.2:c.*172C>A, NM_001007271.1:c.*172C>T, NM_001007271.1:c.*172C>A, NM_001320842.2:c.143C>T, NM_001320842.2:c.143C>A, NM_001320842.1:c.143C>T, NM_001320842.1:c.143C>A, NM_001007273.2:c.143C>T, NM_001007273.2:c.143C>A, NM_001007273.1:c.143C>T, NM_001007273.1:c.143C>A, XM_005269883.4:c.521C>T, XM_005269883.4:c.521C>A, XM_005269883.3:c.521C>T, XM_005269883.3:c.521C>A, XM_005269883.2:c.521C>T, XM_005269883.2:c.521C>A, XM_005269883.1:c.521C>T, XM_005269883.1:c.521C>A, XM_017016314.2:c.521C>T, XM_017016314.2:c.521C>A, XM_017016314.1:c.521C>T, XM_017016314.1:c.521C>A, NM_001007274.1:c.*30C>T, NM_001007274.1:c.*30C>A, NP_001307771.1:p.Ala48Val, NP_001307771.1:p.Ala48Glu, NP_001007274.1:p.Ala48Val, NP_001007274.1:p.Ala48Glu, XP_005269940.1:p.Ala174Val, XP_005269940.1:p.Ala174Glu, XP_016871803.1:p.Ala174Val, XP_016871803.1:p.Ala174Glu

          5.

          rs112032940 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            G>A [Show Flanks]
            Chromosome:
            10:75103972 (GRCh38)
            10:76863730 (GRCh37)
            Canonical SPDI:
            NC_000010.11:75103971:G:A
            Gene:
            DUSP13 (Varview), SAMD8 (Varview)
            Functional Consequence:
            coding_sequence_variant,3_prime_UTR_variant,synonymous_variant,genic_upstream_transcript_variant,intron_variant
            Clinical significance:
            benign
            Validated:
            by frequency,by alfa,by cluster
            MAF:
            A=0.00278/310 (ALFA)
            A=0.00027/1 (TWINSUK)
            A=0.000519/2 (ALSPAC)
            A=0.00318/635 (GnomAD_exomes)
            A=0.009946/312 (ExAC)
            A=0.01418/184 (GoESP)
            A=0.015115/2120 (GnomAD)
            A=0.015327/4057 (TOPMED)
            A=0.016396/82 (1000Genomes)
            G=0.5/1 (SGDP_PRJ)
            HGVS:

            6.

            rs117454002 has merged into rs3088142 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              C>G,T [Show Flanks]
              Chromosome:
              10:75094806 (GRCh38)
              10:76854564 (GRCh37)
              Canonical SPDI:
              NC_000010.11:75094805:C:G,NC_000010.11:75094805:C:T
              Gene:
              DUSP13 (Varview)
              Functional Consequence:
              coding_sequence_variant,genic_downstream_transcript_variant,3_prime_UTR_variant,missense_variant
              Clinical significance:
              benign
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              T=0.447299/165183 (ALFA)
              C=0.082969/152 (Korea1K)
              C=0.0843/247 (KOREAN)
              C=0.087338/1464 (TOMMO)
              C=0.105863/65 (Vietnamese)
              C=0.18595/90 (SGDP_PRJ)
              C=0.25/11 (Siberian)
              T=0.309524/26 (PRJEB36033)
              C=0.317311/24973 (PAGE_STUDY)
              C=0.326271/616 (HapMap)
              C=0.32853/684 (HGDP_Stanford)
              C=0.347222/75 (Qatari)
              T=0.348333/209 (NorthernSweden)
              T=0.35/14 (GENOME_DK)
              C=0.359151/1799 (1000Genomes)
              T=0.404515/1559 (ALSPAC)
              T=0.409655/1519 (TWINSUK)
              T=0.425852/425 (GoNL)
              T=0.439732/1970 (Estonian)
              C=0.445015/117791 (TOPMED)
              T=0.447566/239 (MGP)
              C=0.472658/118483 (GnomAD_exomes)
              C=0.473344/66289 (GnomAD)
              T=0.480132/145 (FINRISK)
              C=0.480922/58004 (ExAC)
              C=0.495156/6440 (GoESP)
              HGVS:
              NC_000010.11:g.75094806C>G, NC_000010.11:g.75094806C>T, NC_000010.10:g.76854564C>G, NC_000010.10:g.76854564C>T, NG_033976.1:g.19407G>C, NG_033976.1:g.19407G>A, NM_016364.3:c.467G>C, NM_016364.3:c.467G>A, NM_001007271.2:c.*775G>C, NM_001007271.2:c.*775G>A, NM_001007271.1:c.*775G>C, NM_001007271.1:c.*775G>A, NM_001320842.2:c.746G>C, NM_001320842.2:c.746G>A, NM_001320842.1:c.746G>C, NM_001320842.1:c.746G>A, NM_001363514.2:c.875G>C, NM_001363514.2:c.875G>A, NM_001363514.1:c.875G>C, NM_001363514.1:c.875G>A, NM_001007273.2:c.746G>C, NM_001007273.2:c.746G>A, NM_001007273.1:c.746G>C, NM_001007273.1:c.746G>A, NM_001320843.2:c.467G>C, NM_001320843.2:c.467G>A, NM_001320843.1:c.467G>C, NM_001320843.1:c.467G>A, NM_001007272.2:c.617G>C, NM_001007272.2:c.617G>A, NM_001007272.1:c.617G>C, NM_001007272.1:c.617G>A, XM_005269883.4:c.1124G>C, XM_005269883.4:c.1124G>A, XM_005269883.3:c.1124G>C, XM_005269883.3:c.1124G>A, XM_005269883.2:c.1124G>C, XM_005269883.2:c.1124G>A, XM_005269883.1:c.1124G>C, XM_005269883.1:c.1124G>A, XM_011539855.3:c.467G>C, XM_011539855.3:c.467G>A, XM_011539855.2:c.467G>C, XM_011539855.2:c.467G>A, XM_011539855.1:c.467G>C, XM_011539855.1:c.467G>A, NM_001007274.1:c.*633G>C, NM_001007274.1:c.*633G>A, NM_001007275.1:c.*529G>C, NM_001007275.1:c.*529G>A, XM_047425305.1:c.467G>C, XM_047425305.1:c.467G>A, XM_047425308.1:c.467G>C, XM_047425308.1:c.467G>A, XM_047425306.1:c.467G>C, XM_047425306.1:c.467G>A, NP_057448.3:p.Cys156Ser, NP_057448.3:p.Cys156Tyr, NP_001307771.1:p.Cys249Ser, NP_001307771.1:p.Cys249Tyr, NP_001350443.1:p.Cys292Ser, NP_001350443.1:p.Cys292Tyr, NP_001007274.1:p.Cys249Ser, NP_001007274.1:p.Cys249Tyr, NP_001307772.1:p.Cys156Ser, NP_001307772.1:p.Cys156Tyr, NP_001007273.1:p.Cys206Ser, NP_001007273.1:p.Cys206Tyr, XP_005269940.1:p.Cys375Ser, XP_005269940.1:p.Cys375Tyr, XP_011538157.1:p.Cys156Ser, XP_011538157.1:p.Cys156Tyr, XP_047281261.1:p.Cys156Ser, XP_047281261.1:p.Cys156Tyr, XP_047281264.1:p.Cys156Ser, XP_047281264.1:p.Cys156Tyr, XP_047281262.1:p.Cys156Ser, XP_047281262.1:p.Cys156Tyr

              7.

              rs59052514 has merged into rs3088142 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                C>G,T [Show Flanks]
                Chromosome:
                10:75094806 (GRCh38)
                10:76854564 (GRCh37)
                Canonical SPDI:
                NC_000010.11:75094805:C:G,NC_000010.11:75094805:C:T
                Gene:
                DUSP13 (Varview)
                Functional Consequence:
                coding_sequence_variant,genic_downstream_transcript_variant,3_prime_UTR_variant,missense_variant
                Clinical significance:
                benign
                Validated:
                by frequency,by alfa,by cluster
                MAF:
                T=0.447299/165183 (ALFA)
                C=0.082969/152 (Korea1K)
                C=0.0843/247 (KOREAN)
                C=0.087338/1464 (TOMMO)
                C=0.105863/65 (Vietnamese)
                C=0.18595/90 (SGDP_PRJ)
                C=0.25/11 (Siberian)
                T=0.309524/26 (PRJEB36033)
                C=0.317311/24973 (PAGE_STUDY)
                C=0.326271/616 (HapMap)
                C=0.32853/684 (HGDP_Stanford)
                C=0.347222/75 (Qatari)
                T=0.348333/209 (NorthernSweden)
                T=0.35/14 (GENOME_DK)
                C=0.359151/1799 (1000Genomes)
                T=0.404515/1559 (ALSPAC)
                T=0.409655/1519 (TWINSUK)
                T=0.425852/425 (GoNL)
                T=0.439732/1970 (Estonian)
                C=0.445015/117791 (TOPMED)
                T=0.447566/239 (MGP)
                C=0.472658/118483 (GnomAD_exomes)
                C=0.473344/66289 (GnomAD)
                T=0.480132/145 (FINRISK)
                C=0.480922/58004 (ExAC)
                C=0.495156/6440 (GoESP)
                HGVS:
                NC_000010.11:g.75094806C>G, NC_000010.11:g.75094806C>T, NC_000010.10:g.76854564C>G, NC_000010.10:g.76854564C>T, NG_033976.1:g.19407G>C, NG_033976.1:g.19407G>A, NM_016364.3:c.467G>C, NM_016364.3:c.467G>A, NM_001007271.2:c.*775G>C, NM_001007271.2:c.*775G>A, NM_001007271.1:c.*775G>C, NM_001007271.1:c.*775G>A, NM_001320842.2:c.746G>C, NM_001320842.2:c.746G>A, NM_001320842.1:c.746G>C, NM_001320842.1:c.746G>A, NM_001363514.2:c.875G>C, NM_001363514.2:c.875G>A, NM_001363514.1:c.875G>C, NM_001363514.1:c.875G>A, NM_001007273.2:c.746G>C, NM_001007273.2:c.746G>A, NM_001007273.1:c.746G>C, NM_001007273.1:c.746G>A, NM_001320843.2:c.467G>C, NM_001320843.2:c.467G>A, NM_001320843.1:c.467G>C, NM_001320843.1:c.467G>A, NM_001007272.2:c.617G>C, NM_001007272.2:c.617G>A, NM_001007272.1:c.617G>C, NM_001007272.1:c.617G>A, XM_005269883.4:c.1124G>C, XM_005269883.4:c.1124G>A, XM_005269883.3:c.1124G>C, XM_005269883.3:c.1124G>A, XM_005269883.2:c.1124G>C, XM_005269883.2:c.1124G>A, XM_005269883.1:c.1124G>C, XM_005269883.1:c.1124G>A, XM_011539855.3:c.467G>C, XM_011539855.3:c.467G>A, XM_011539855.2:c.467G>C, XM_011539855.2:c.467G>A, XM_011539855.1:c.467G>C, XM_011539855.1:c.467G>A, NM_001007274.1:c.*633G>C, NM_001007274.1:c.*633G>A, NM_001007275.1:c.*529G>C, NM_001007275.1:c.*529G>A, XM_047425305.1:c.467G>C, XM_047425305.1:c.467G>A, XM_047425308.1:c.467G>C, XM_047425308.1:c.467G>A, XM_047425306.1:c.467G>C, XM_047425306.1:c.467G>A, NP_057448.3:p.Cys156Ser, NP_057448.3:p.Cys156Tyr, NP_001307771.1:p.Cys249Ser, NP_001307771.1:p.Cys249Tyr, NP_001350443.1:p.Cys292Ser, NP_001350443.1:p.Cys292Tyr, NP_001007274.1:p.Cys249Ser, NP_001007274.1:p.Cys249Tyr, NP_001307772.1:p.Cys156Ser, NP_001307772.1:p.Cys156Tyr, NP_001007273.1:p.Cys206Ser, NP_001007273.1:p.Cys206Tyr, XP_005269940.1:p.Cys375Ser, XP_005269940.1:p.Cys375Tyr, XP_011538157.1:p.Cys156Ser, XP_011538157.1:p.Cys156Tyr, XP_047281261.1:p.Cys156Ser, XP_047281261.1:p.Cys156Tyr, XP_047281264.1:p.Cys156Ser, XP_047281264.1:p.Cys156Tyr, XP_047281262.1:p.Cys156Ser, XP_047281262.1:p.Cys156Tyr

                8.

                rs52833294 has merged into rs3088142 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  C>G,T [Show Flanks]
                  Chromosome:
                  10:75094806 (GRCh38)
                  10:76854564 (GRCh37)
                  Canonical SPDI:
                  NC_000010.11:75094805:C:G,NC_000010.11:75094805:C:T
                  Gene:
                  DUSP13 (Varview)
                  Functional Consequence:
                  coding_sequence_variant,genic_downstream_transcript_variant,3_prime_UTR_variant,missense_variant
                  Clinical significance:
                  benign
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  T=0.447299/165183 (ALFA)
                  C=0.082969/152 (Korea1K)
                  C=0.0843/247 (KOREAN)
                  C=0.087338/1464 (TOMMO)
                  C=0.105863/65 (Vietnamese)
                  C=0.18595/90 (SGDP_PRJ)
                  C=0.25/11 (Siberian)
                  T=0.309524/26 (PRJEB36033)
                  C=0.317311/24973 (PAGE_STUDY)
                  C=0.326271/616 (HapMap)
                  C=0.32853/684 (HGDP_Stanford)
                  C=0.347222/75 (Qatari)
                  T=0.348333/209 (NorthernSweden)
                  T=0.35/14 (GENOME_DK)
                  C=0.359151/1799 (1000Genomes)
                  T=0.404515/1559 (ALSPAC)
                  T=0.409655/1519 (TWINSUK)
                  T=0.425852/425 (GoNL)
                  T=0.439732/1970 (Estonian)
                  C=0.445015/117791 (TOPMED)
                  T=0.447566/239 (MGP)
                  C=0.472658/118483 (GnomAD_exomes)
                  C=0.473344/66289 (GnomAD)
                  T=0.480132/145 (FINRISK)
                  C=0.480922/58004 (ExAC)
                  C=0.495156/6440 (GoESP)
                  HGVS:
                  NC_000010.11:g.75094806C>G, NC_000010.11:g.75094806C>T, NC_000010.10:g.76854564C>G, NC_000010.10:g.76854564C>T, NG_033976.1:g.19407G>C, NG_033976.1:g.19407G>A, NM_016364.3:c.467G>C, NM_016364.3:c.467G>A, NM_001007271.2:c.*775G>C, NM_001007271.2:c.*775G>A, NM_001007271.1:c.*775G>C, NM_001007271.1:c.*775G>A, NM_001320842.2:c.746G>C, NM_001320842.2:c.746G>A, NM_001320842.1:c.746G>C, NM_001320842.1:c.746G>A, NM_001363514.2:c.875G>C, NM_001363514.2:c.875G>A, NM_001363514.1:c.875G>C, NM_001363514.1:c.875G>A, NM_001007273.2:c.746G>C, NM_001007273.2:c.746G>A, NM_001007273.1:c.746G>C, NM_001007273.1:c.746G>A, NM_001320843.2:c.467G>C, NM_001320843.2:c.467G>A, NM_001320843.1:c.467G>C, NM_001320843.1:c.467G>A, NM_001007272.2:c.617G>C, NM_001007272.2:c.617G>A, NM_001007272.1:c.617G>C, NM_001007272.1:c.617G>A, XM_005269883.4:c.1124G>C, XM_005269883.4:c.1124G>A, XM_005269883.3:c.1124G>C, XM_005269883.3:c.1124G>A, XM_005269883.2:c.1124G>C, XM_005269883.2:c.1124G>A, XM_005269883.1:c.1124G>C, XM_005269883.1:c.1124G>A, XM_011539855.3:c.467G>C, XM_011539855.3:c.467G>A, XM_011539855.2:c.467G>C, XM_011539855.2:c.467G>A, XM_011539855.1:c.467G>C, XM_011539855.1:c.467G>A, NM_001007274.1:c.*633G>C, NM_001007274.1:c.*633G>A, NM_001007275.1:c.*529G>C, NM_001007275.1:c.*529G>A, XM_047425305.1:c.467G>C, XM_047425305.1:c.467G>A, XM_047425308.1:c.467G>C, XM_047425308.1:c.467G>A, XM_047425306.1:c.467G>C, XM_047425306.1:c.467G>A, NP_057448.3:p.Cys156Ser, NP_057448.3:p.Cys156Tyr, NP_001307771.1:p.Cys249Ser, NP_001307771.1:p.Cys249Tyr, NP_001350443.1:p.Cys292Ser, NP_001350443.1:p.Cys292Tyr, NP_001007274.1:p.Cys249Ser, NP_001007274.1:p.Cys249Tyr, NP_001307772.1:p.Cys156Ser, NP_001307772.1:p.Cys156Tyr, NP_001007273.1:p.Cys206Ser, NP_001007273.1:p.Cys206Tyr, XP_005269940.1:p.Cys375Ser, XP_005269940.1:p.Cys375Tyr, XP_011538157.1:p.Cys156Ser, XP_011538157.1:p.Cys156Tyr, XP_047281261.1:p.Cys156Ser, XP_047281261.1:p.Cys156Tyr, XP_047281264.1:p.Cys156Ser, XP_047281264.1:p.Cys156Tyr, XP_047281262.1:p.Cys156Ser, XP_047281262.1:p.Cys156Tyr

                  9.

                  rs17858059 has merged into rs3088142 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    C>G,T [Show Flanks]
                    Chromosome:
                    10:75094806 (GRCh38)
                    10:76854564 (GRCh37)
                    Canonical SPDI:
                    NC_000010.11:75094805:C:G,NC_000010.11:75094805:C:T
                    Gene:
                    DUSP13 (Varview)
                    Functional Consequence:
                    coding_sequence_variant,genic_downstream_transcript_variant,3_prime_UTR_variant,missense_variant
                    Clinical significance:
                    benign
                    Validated:
                    by frequency,by alfa,by cluster
                    MAF:
                    T=0.447299/165183 (ALFA)
                    C=0.082969/152 (Korea1K)
                    C=0.0843/247 (KOREAN)
                    C=0.087338/1464 (TOMMO)
                    C=0.105863/65 (Vietnamese)
                    C=0.18595/90 (SGDP_PRJ)
                    C=0.25/11 (Siberian)
                    T=0.309524/26 (PRJEB36033)
                    C=0.317311/24973 (PAGE_STUDY)
                    C=0.326271/616 (HapMap)
                    C=0.32853/684 (HGDP_Stanford)
                    C=0.347222/75 (Qatari)
                    T=0.348333/209 (NorthernSweden)
                    T=0.35/14 (GENOME_DK)
                    C=0.359151/1799 (1000Genomes)
                    T=0.404515/1559 (ALSPAC)
                    T=0.409655/1519 (TWINSUK)
                    T=0.425852/425 (GoNL)
                    T=0.439732/1970 (Estonian)
                    C=0.445015/117791 (TOPMED)
                    T=0.447566/239 (MGP)
                    C=0.472658/118483 (GnomAD_exomes)
                    C=0.473344/66289 (GnomAD)
                    T=0.480132/145 (FINRISK)
                    C=0.480922/58004 (ExAC)
                    C=0.495156/6440 (GoESP)
                    HGVS:
                    NC_000010.11:g.75094806C>G, NC_000010.11:g.75094806C>T, NC_000010.10:g.76854564C>G, NC_000010.10:g.76854564C>T, NG_033976.1:g.19407G>C, NG_033976.1:g.19407G>A, NM_016364.3:c.467G>C, NM_016364.3:c.467G>A, NM_001007271.2:c.*775G>C, NM_001007271.2:c.*775G>A, NM_001007271.1:c.*775G>C, NM_001007271.1:c.*775G>A, NM_001320842.2:c.746G>C, NM_001320842.2:c.746G>A, NM_001320842.1:c.746G>C, NM_001320842.1:c.746G>A, NM_001363514.2:c.875G>C, NM_001363514.2:c.875G>A, NM_001363514.1:c.875G>C, NM_001363514.1:c.875G>A, NM_001007273.2:c.746G>C, NM_001007273.2:c.746G>A, NM_001007273.1:c.746G>C, NM_001007273.1:c.746G>A, NM_001320843.2:c.467G>C, NM_001320843.2:c.467G>A, NM_001320843.1:c.467G>C, NM_001320843.1:c.467G>A, NM_001007272.2:c.617G>C, NM_001007272.2:c.617G>A, NM_001007272.1:c.617G>C, NM_001007272.1:c.617G>A, XM_005269883.4:c.1124G>C, XM_005269883.4:c.1124G>A, XM_005269883.3:c.1124G>C, XM_005269883.3:c.1124G>A, XM_005269883.2:c.1124G>C, XM_005269883.2:c.1124G>A, XM_005269883.1:c.1124G>C, XM_005269883.1:c.1124G>A, XM_011539855.3:c.467G>C, XM_011539855.3:c.467G>A, XM_011539855.2:c.467G>C, XM_011539855.2:c.467G>A, XM_011539855.1:c.467G>C, XM_011539855.1:c.467G>A, NM_001007274.1:c.*633G>C, NM_001007274.1:c.*633G>A, NM_001007275.1:c.*529G>C, NM_001007275.1:c.*529G>A, XM_047425305.1:c.467G>C, XM_047425305.1:c.467G>A, XM_047425308.1:c.467G>C, XM_047425308.1:c.467G>A, XM_047425306.1:c.467G>C, XM_047425306.1:c.467G>A, NP_057448.3:p.Cys156Ser, NP_057448.3:p.Cys156Tyr, NP_001307771.1:p.Cys249Ser, NP_001307771.1:p.Cys249Tyr, NP_001350443.1:p.Cys292Ser, NP_001350443.1:p.Cys292Tyr, NP_001007274.1:p.Cys249Ser, NP_001007274.1:p.Cys249Tyr, NP_001307772.1:p.Cys156Ser, NP_001307772.1:p.Cys156Tyr, NP_001007273.1:p.Cys206Ser, NP_001007273.1:p.Cys206Tyr, XP_005269940.1:p.Cys375Ser, XP_005269940.1:p.Cys375Tyr, XP_011538157.1:p.Cys156Ser, XP_011538157.1:p.Cys156Tyr, XP_047281261.1:p.Cys156Ser, XP_047281261.1:p.Cys156Tyr, XP_047281264.1:p.Cys156Ser, XP_047281264.1:p.Cys156Tyr, XP_047281262.1:p.Cys156Ser, XP_047281262.1:p.Cys156Tyr

                    10.

                    rs17845242 has merged into rs3088142 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      C>G,T [Show Flanks]
                      Chromosome:
                      10:75094806 (GRCh38)
                      10:76854564 (GRCh37)
                      Canonical SPDI:
                      NC_000010.11:75094805:C:G,NC_000010.11:75094805:C:T
                      Gene:
                      DUSP13 (Varview)
                      Functional Consequence:
                      coding_sequence_variant,genic_downstream_transcript_variant,3_prime_UTR_variant,missense_variant
                      Clinical significance:
                      benign
                      Validated:
                      by frequency,by alfa,by cluster
                      MAF:
                      T=0.447299/165183 (ALFA)
                      C=0.082969/152 (Korea1K)
                      C=0.0843/247 (KOREAN)
                      C=0.087338/1464 (TOMMO)
                      C=0.105863/65 (Vietnamese)
                      C=0.18595/90 (SGDP_PRJ)
                      C=0.25/11 (Siberian)
                      T=0.309524/26 (PRJEB36033)
                      C=0.317311/24973 (PAGE_STUDY)
                      C=0.326271/616 (HapMap)
                      C=0.32853/684 (HGDP_Stanford)
                      C=0.347222/75 (Qatari)
                      T=0.348333/209 (NorthernSweden)
                      T=0.35/14 (GENOME_DK)
                      C=0.359151/1799 (1000Genomes)
                      T=0.404515/1559 (ALSPAC)
                      T=0.409655/1519 (TWINSUK)
                      T=0.425852/425 (GoNL)
                      T=0.439732/1970 (Estonian)
                      C=0.445015/117791 (TOPMED)
                      T=0.447566/239 (MGP)
                      C=0.472658/118483 (GnomAD_exomes)
                      C=0.473344/66289 (GnomAD)
                      T=0.480132/145 (FINRISK)
                      C=0.480922/58004 (ExAC)
                      C=0.495156/6440 (GoESP)
                      HGVS:
                      NC_000010.11:g.75094806C>G, NC_000010.11:g.75094806C>T, NC_000010.10:g.76854564C>G, NC_000010.10:g.76854564C>T, NG_033976.1:g.19407G>C, NG_033976.1:g.19407G>A, NM_016364.3:c.467G>C, NM_016364.3:c.467G>A, NM_001007271.2:c.*775G>C, NM_001007271.2:c.*775G>A, NM_001007271.1:c.*775G>C, NM_001007271.1:c.*775G>A, NM_001320842.2:c.746G>C, NM_001320842.2:c.746G>A, NM_001320842.1:c.746G>C, NM_001320842.1:c.746G>A, NM_001363514.2:c.875G>C, NM_001363514.2:c.875G>A, NM_001363514.1:c.875G>C, NM_001363514.1:c.875G>A, NM_001007273.2:c.746G>C, NM_001007273.2:c.746G>A, NM_001007273.1:c.746G>C, NM_001007273.1:c.746G>A, NM_001320843.2:c.467G>C, NM_001320843.2:c.467G>A, NM_001320843.1:c.467G>C, NM_001320843.1:c.467G>A, NM_001007272.2:c.617G>C, NM_001007272.2:c.617G>A, NM_001007272.1:c.617G>C, NM_001007272.1:c.617G>A, XM_005269883.4:c.1124G>C, XM_005269883.4:c.1124G>A, XM_005269883.3:c.1124G>C, XM_005269883.3:c.1124G>A, XM_005269883.2:c.1124G>C, XM_005269883.2:c.1124G>A, XM_005269883.1:c.1124G>C, XM_005269883.1:c.1124G>A, XM_011539855.3:c.467G>C, XM_011539855.3:c.467G>A, XM_011539855.2:c.467G>C, XM_011539855.2:c.467G>A, XM_011539855.1:c.467G>C, XM_011539855.1:c.467G>A, NM_001007274.1:c.*633G>C, NM_001007274.1:c.*633G>A, NM_001007275.1:c.*529G>C, NM_001007275.1:c.*529G>A, XM_047425305.1:c.467G>C, XM_047425305.1:c.467G>A, XM_047425308.1:c.467G>C, XM_047425308.1:c.467G>A, XM_047425306.1:c.467G>C, XM_047425306.1:c.467G>A, NP_057448.3:p.Cys156Ser, NP_057448.3:p.Cys156Tyr, NP_001307771.1:p.Cys249Ser, NP_001307771.1:p.Cys249Tyr, NP_001350443.1:p.Cys292Ser, NP_001350443.1:p.Cys292Tyr, NP_001007274.1:p.Cys249Ser, NP_001007274.1:p.Cys249Tyr, NP_001307772.1:p.Cys156Ser, NP_001307772.1:p.Cys156Tyr, NP_001007273.1:p.Cys206Ser, NP_001007273.1:p.Cys206Tyr, XP_005269940.1:p.Cys375Ser, XP_005269940.1:p.Cys375Tyr, XP_011538157.1:p.Cys156Ser, XP_011538157.1:p.Cys156Tyr, XP_047281261.1:p.Cys156Ser, XP_047281261.1:p.Cys156Tyr, XP_047281264.1:p.Cys156Ser, XP_047281264.1:p.Cys156Tyr, XP_047281262.1:p.Cys156Ser, XP_047281262.1:p.Cys156Tyr

                      11.

                      rs17688755 has merged into rs3088142 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        C>G,T [Show Flanks]
                        Chromosome:
                        10:75094806 (GRCh38)
                        10:76854564 (GRCh37)
                        Canonical SPDI:
                        NC_000010.11:75094805:C:G,NC_000010.11:75094805:C:T
                        Gene:
                        DUSP13 (Varview)
                        Functional Consequence:
                        coding_sequence_variant,genic_downstream_transcript_variant,3_prime_UTR_variant,missense_variant
                        Clinical significance:
                        benign
                        Validated:
                        by frequency,by alfa,by cluster
                        MAF:
                        T=0.447299/165183 (ALFA)
                        C=0.082969/152 (Korea1K)
                        C=0.0843/247 (KOREAN)
                        C=0.087338/1464 (TOMMO)
                        C=0.105863/65 (Vietnamese)
                        C=0.18595/90 (SGDP_PRJ)
                        C=0.25/11 (Siberian)
                        T=0.309524/26 (PRJEB36033)
                        C=0.317311/24973 (PAGE_STUDY)
                        C=0.326271/616 (HapMap)
                        C=0.32853/684 (HGDP_Stanford)
                        C=0.347222/75 (Qatari)
                        T=0.348333/209 (NorthernSweden)
                        T=0.35/14 (GENOME_DK)
                        C=0.359151/1799 (1000Genomes)
                        T=0.404515/1559 (ALSPAC)
                        T=0.409655/1519 (TWINSUK)
                        T=0.425852/425 (GoNL)
                        T=0.439732/1970 (Estonian)
                        C=0.445015/117791 (TOPMED)
                        T=0.447566/239 (MGP)
                        C=0.472658/118483 (GnomAD_exomes)
                        C=0.473344/66289 (GnomAD)
                        T=0.480132/145 (FINRISK)
                        C=0.480922/58004 (ExAC)
                        C=0.495156/6440 (GoESP)
                        HGVS:
                        NC_000010.11:g.75094806C>G, NC_000010.11:g.75094806C>T, NC_000010.10:g.76854564C>G, NC_000010.10:g.76854564C>T, NG_033976.1:g.19407G>C, NG_033976.1:g.19407G>A, NM_016364.3:c.467G>C, NM_016364.3:c.467G>A, NM_001007271.2:c.*775G>C, NM_001007271.2:c.*775G>A, NM_001007271.1:c.*775G>C, NM_001007271.1:c.*775G>A, NM_001320842.2:c.746G>C, NM_001320842.2:c.746G>A, NM_001320842.1:c.746G>C, NM_001320842.1:c.746G>A, NM_001363514.2:c.875G>C, NM_001363514.2:c.875G>A, NM_001363514.1:c.875G>C, NM_001363514.1:c.875G>A, NM_001007273.2:c.746G>C, NM_001007273.2:c.746G>A, NM_001007273.1:c.746G>C, NM_001007273.1:c.746G>A, NM_001320843.2:c.467G>C, NM_001320843.2:c.467G>A, NM_001320843.1:c.467G>C, NM_001320843.1:c.467G>A, NM_001007272.2:c.617G>C, NM_001007272.2:c.617G>A, NM_001007272.1:c.617G>C, NM_001007272.1:c.617G>A, XM_005269883.4:c.1124G>C, XM_005269883.4:c.1124G>A, XM_005269883.3:c.1124G>C, XM_005269883.3:c.1124G>A, XM_005269883.2:c.1124G>C, XM_005269883.2:c.1124G>A, XM_005269883.1:c.1124G>C, XM_005269883.1:c.1124G>A, XM_011539855.3:c.467G>C, XM_011539855.3:c.467G>A, XM_011539855.2:c.467G>C, XM_011539855.2:c.467G>A, XM_011539855.1:c.467G>C, XM_011539855.1:c.467G>A, NM_001007274.1:c.*633G>C, NM_001007274.1:c.*633G>A, NM_001007275.1:c.*529G>C, NM_001007275.1:c.*529G>A, XM_047425305.1:c.467G>C, XM_047425305.1:c.467G>A, XM_047425308.1:c.467G>C, XM_047425308.1:c.467G>A, XM_047425306.1:c.467G>C, XM_047425306.1:c.467G>A, NP_057448.3:p.Cys156Ser, NP_057448.3:p.Cys156Tyr, NP_001307771.1:p.Cys249Ser, NP_001307771.1:p.Cys249Tyr, NP_001350443.1:p.Cys292Ser, NP_001350443.1:p.Cys292Tyr, NP_001007274.1:p.Cys249Ser, NP_001007274.1:p.Cys249Tyr, NP_001307772.1:p.Cys156Ser, NP_001307772.1:p.Cys156Tyr, NP_001007273.1:p.Cys206Ser, NP_001007273.1:p.Cys206Tyr, XP_005269940.1:p.Cys375Ser, XP_005269940.1:p.Cys375Tyr, XP_011538157.1:p.Cys156Ser, XP_011538157.1:p.Cys156Tyr, XP_047281261.1:p.Cys156Ser, XP_047281261.1:p.Cys156Tyr, XP_047281264.1:p.Cys156Ser, XP_047281264.1:p.Cys156Tyr, XP_047281262.1:p.Cys156Ser, XP_047281262.1:p.Cys156Tyr

                        12.

                        rs3740320 has merged into rs3088142 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          C>G,T [Show Flanks]
                          Chromosome:
                          10:75094806 (GRCh38)
                          10:76854564 (GRCh37)
                          Canonical SPDI:
                          NC_000010.11:75094805:C:G,NC_000010.11:75094805:C:T
                          Gene:
                          DUSP13 (Varview)
                          Functional Consequence:
                          coding_sequence_variant,genic_downstream_transcript_variant,3_prime_UTR_variant,missense_variant
                          Clinical significance:
                          benign
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          T=0.447299/165183 (ALFA)
                          C=0.082969/152 (Korea1K)
                          C=0.0843/247 (KOREAN)
                          C=0.087338/1464 (TOMMO)
                          C=0.105863/65 (Vietnamese)
                          C=0.18595/90 (SGDP_PRJ)
                          C=0.25/11 (Siberian)
                          T=0.309524/26 (PRJEB36033)
                          C=0.317311/24973 (PAGE_STUDY)
                          C=0.326271/616 (HapMap)
                          C=0.32853/684 (HGDP_Stanford)
                          C=0.347222/75 (Qatari)
                          T=0.348333/209 (NorthernSweden)
                          T=0.35/14 (GENOME_DK)
                          C=0.359151/1799 (1000Genomes)
                          T=0.404515/1559 (ALSPAC)
                          T=0.409655/1519 (TWINSUK)
                          T=0.425852/425 (GoNL)
                          T=0.439732/1970 (Estonian)
                          C=0.445015/117791 (TOPMED)
                          T=0.447566/239 (MGP)
                          C=0.472658/118483 (GnomAD_exomes)
                          C=0.473344/66289 (GnomAD)
                          T=0.480132/145 (FINRISK)
                          C=0.480922/58004 (ExAC)
                          C=0.495156/6440 (GoESP)
                          HGVS:
                          NC_000010.11:g.75094806C>G, NC_000010.11:g.75094806C>T, NC_000010.10:g.76854564C>G, NC_000010.10:g.76854564C>T, NG_033976.1:g.19407G>C, NG_033976.1:g.19407G>A, NM_016364.3:c.467G>C, NM_016364.3:c.467G>A, NM_001007271.2:c.*775G>C, NM_001007271.2:c.*775G>A, NM_001007271.1:c.*775G>C, NM_001007271.1:c.*775G>A, NM_001320842.2:c.746G>C, NM_001320842.2:c.746G>A, NM_001320842.1:c.746G>C, NM_001320842.1:c.746G>A, NM_001363514.2:c.875G>C, NM_001363514.2:c.875G>A, NM_001363514.1:c.875G>C, NM_001363514.1:c.875G>A, NM_001007273.2:c.746G>C, NM_001007273.2:c.746G>A, NM_001007273.1:c.746G>C, NM_001007273.1:c.746G>A, NM_001320843.2:c.467G>C, NM_001320843.2:c.467G>A, NM_001320843.1:c.467G>C, NM_001320843.1:c.467G>A, NM_001007272.2:c.617G>C, NM_001007272.2:c.617G>A, NM_001007272.1:c.617G>C, NM_001007272.1:c.617G>A, XM_005269883.4:c.1124G>C, XM_005269883.4:c.1124G>A, XM_005269883.3:c.1124G>C, XM_005269883.3:c.1124G>A, XM_005269883.2:c.1124G>C, XM_005269883.2:c.1124G>A, XM_005269883.1:c.1124G>C, XM_005269883.1:c.1124G>A, XM_011539855.3:c.467G>C, XM_011539855.3:c.467G>A, XM_011539855.2:c.467G>C, XM_011539855.2:c.467G>A, XM_011539855.1:c.467G>C, XM_011539855.1:c.467G>A, NM_001007274.1:c.*633G>C, NM_001007274.1:c.*633G>A, NM_001007275.1:c.*529G>C, NM_001007275.1:c.*529G>A, XM_047425305.1:c.467G>C, XM_047425305.1:c.467G>A, XM_047425308.1:c.467G>C, XM_047425308.1:c.467G>A, XM_047425306.1:c.467G>C, XM_047425306.1:c.467G>A, NP_057448.3:p.Cys156Ser, NP_057448.3:p.Cys156Tyr, NP_001307771.1:p.Cys249Ser, NP_001307771.1:p.Cys249Tyr, NP_001350443.1:p.Cys292Ser, NP_001350443.1:p.Cys292Tyr, NP_001007274.1:p.Cys249Ser, NP_001007274.1:p.Cys249Tyr, NP_001307772.1:p.Cys156Ser, NP_001307772.1:p.Cys156Tyr, NP_001007273.1:p.Cys206Ser, NP_001007273.1:p.Cys206Tyr, XP_005269940.1:p.Cys375Ser, XP_005269940.1:p.Cys375Tyr, XP_011538157.1:p.Cys156Ser, XP_011538157.1:p.Cys156Tyr, XP_047281261.1:p.Cys156Ser, XP_047281261.1:p.Cys156Tyr, XP_047281264.1:p.Cys156Ser, XP_047281264.1:p.Cys156Tyr, XP_047281262.1:p.Cys156Ser, XP_047281262.1:p.Cys156Tyr

                          13.

                          rs3199830 has merged into rs3088142 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            C>G,T [Show Flanks]
                            Chromosome:
                            10:75094806 (GRCh38)
                            10:76854564 (GRCh37)
                            Canonical SPDI:
                            NC_000010.11:75094805:C:G,NC_000010.11:75094805:C:T
                            Gene:
                            DUSP13 (Varview)
                            Functional Consequence:
                            coding_sequence_variant,genic_downstream_transcript_variant,3_prime_UTR_variant,missense_variant
                            Clinical significance:
                            benign
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            T=0.447299/165183 (ALFA)
                            C=0.082969/152 (Korea1K)
                            C=0.0843/247 (KOREAN)
                            C=0.087338/1464 (TOMMO)
                            C=0.105863/65 (Vietnamese)
                            C=0.18595/90 (SGDP_PRJ)
                            C=0.25/11 (Siberian)
                            T=0.309524/26 (PRJEB36033)
                            C=0.317311/24973 (PAGE_STUDY)
                            C=0.326271/616 (HapMap)
                            C=0.32853/684 (HGDP_Stanford)
                            C=0.347222/75 (Qatari)
                            T=0.348333/209 (NorthernSweden)
                            T=0.35/14 (GENOME_DK)
                            C=0.359151/1799 (1000Genomes)
                            T=0.404515/1559 (ALSPAC)
                            T=0.409655/1519 (TWINSUK)
                            T=0.425852/425 (GoNL)
                            T=0.439732/1970 (Estonian)
                            C=0.445015/117791 (TOPMED)
                            T=0.447566/239 (MGP)
                            C=0.472658/118483 (GnomAD_exomes)
                            C=0.473344/66289 (GnomAD)
                            T=0.480132/145 (FINRISK)
                            C=0.480922/58004 (ExAC)
                            C=0.495156/6440 (GoESP)
                            HGVS:
                            NC_000010.11:g.75094806C>G, NC_000010.11:g.75094806C>T, NC_000010.10:g.76854564C>G, NC_000010.10:g.76854564C>T, NG_033976.1:g.19407G>C, NG_033976.1:g.19407G>A, NM_016364.3:c.467G>C, NM_016364.3:c.467G>A, NM_001007271.2:c.*775G>C, NM_001007271.2:c.*775G>A, NM_001007271.1:c.*775G>C, NM_001007271.1:c.*775G>A, NM_001320842.2:c.746G>C, NM_001320842.2:c.746G>A, NM_001320842.1:c.746G>C, NM_001320842.1:c.746G>A, NM_001363514.2:c.875G>C, NM_001363514.2:c.875G>A, NM_001363514.1:c.875G>C, NM_001363514.1:c.875G>A, NM_001007273.2:c.746G>C, NM_001007273.2:c.746G>A, NM_001007273.1:c.746G>C, NM_001007273.1:c.746G>A, NM_001320843.2:c.467G>C, NM_001320843.2:c.467G>A, NM_001320843.1:c.467G>C, NM_001320843.1:c.467G>A, NM_001007272.2:c.617G>C, NM_001007272.2:c.617G>A, NM_001007272.1:c.617G>C, NM_001007272.1:c.617G>A, XM_005269883.4:c.1124G>C, XM_005269883.4:c.1124G>A, XM_005269883.3:c.1124G>C, XM_005269883.3:c.1124G>A, XM_005269883.2:c.1124G>C, XM_005269883.2:c.1124G>A, XM_005269883.1:c.1124G>C, XM_005269883.1:c.1124G>A, XM_011539855.3:c.467G>C, XM_011539855.3:c.467G>A, XM_011539855.2:c.467G>C, XM_011539855.2:c.467G>A, XM_011539855.1:c.467G>C, XM_011539855.1:c.467G>A, NM_001007274.1:c.*633G>C, NM_001007274.1:c.*633G>A, NM_001007275.1:c.*529G>C, NM_001007275.1:c.*529G>A, XM_047425305.1:c.467G>C, XM_047425305.1:c.467G>A, XM_047425308.1:c.467G>C, XM_047425308.1:c.467G>A, XM_047425306.1:c.467G>C, XM_047425306.1:c.467G>A, NP_057448.3:p.Cys156Ser, NP_057448.3:p.Cys156Tyr, NP_001307771.1:p.Cys249Ser, NP_001307771.1:p.Cys249Tyr, NP_001350443.1:p.Cys292Ser, NP_001350443.1:p.Cys292Tyr, NP_001007274.1:p.Cys249Ser, NP_001007274.1:p.Cys249Tyr, NP_001307772.1:p.Cys156Ser, NP_001307772.1:p.Cys156Tyr, NP_001007273.1:p.Cys206Ser, NP_001007273.1:p.Cys206Tyr, XP_005269940.1:p.Cys375Ser, XP_005269940.1:p.Cys375Tyr, XP_011538157.1:p.Cys156Ser, XP_011538157.1:p.Cys156Tyr, XP_047281261.1:p.Cys156Ser, XP_047281261.1:p.Cys156Tyr, XP_047281264.1:p.Cys156Ser, XP_047281264.1:p.Cys156Tyr, XP_047281262.1:p.Cys156Ser, XP_047281262.1:p.Cys156Tyr

                            14.

                            rs52804188 has merged into rs16931996 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              G>A,C [Show Flanks]
                              Chromosome:
                              10:75094705 (GRCh38)
                              10:76854463 (GRCh37)
                              Canonical SPDI:
                              NC_000010.11:75094704:G:A,NC_000010.11:75094704:G:C
                              Gene:
                              DUSP13 (Varview)
                              Functional Consequence:
                              genic_downstream_transcript_variant,coding_sequence_variant,stop_gained,missense_variant,3_prime_UTR_variant
                              Clinical significance:
                              benign
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              C=0.002456/270 (ALFA)
                              C=0.000259/1 (ALSPAC)
                              C=0.000539/2 (TWINSUK)
                              C=0.001002/1 (GoNL)
                              C=0.001263/1 (PRJEB37584)
                              C=0.001873/1 (MGP)
                              C=0.030762/154 (1000Genomes)
                              C=0.031897/4472 (GnomAD)
                              C=0.033688/8917 (TOPMED)
                              C=0.035753/465 (GoESP)
                              C=0.037037/8 (Qatari)
                              C=0.042424/14 (HapMap)
                              G=0.5/12 (SGDP_PRJ)
                              HGVS:
                              NC_000010.11:g.75094705G>A, NC_000010.11:g.75094705G>C, NC_000010.10:g.76854463G>A, NC_000010.10:g.76854463G>C, NG_033976.1:g.19508C>T, NG_033976.1:g.19508C>G, NM_016364.3:c.568C>T, NM_016364.3:c.568C>G, NM_001007271.2:c.*876C>T, NM_001007271.2:c.*876C>G, NM_001007271.1:c.*876C>T, NM_001007271.1:c.*876C>G, NM_001320842.2:c.847C>T, NM_001320842.2:c.847C>G, NM_001320842.1:c.847C>T, NM_001320842.1:c.847C>G, NM_001363514.2:c.976C>T, NM_001363514.2:c.976C>G, NM_001363514.1:c.976C>T, NM_001363514.1:c.976C>G, NM_001007273.2:c.847C>T, NM_001007273.2:c.847C>G, NM_001007273.1:c.847C>T, NM_001007273.1:c.847C>G, NM_001320843.2:c.568C>T, NM_001320843.2:c.568C>G, NM_001320843.1:c.568C>T, NM_001320843.1:c.568C>G, NM_001007272.2:c.718C>T, NM_001007272.2:c.718C>G, NM_001007272.1:c.718C>T, NM_001007272.1:c.718C>G, XM_005269883.4:c.1225C>T, XM_005269883.4:c.1225C>G, XM_005269883.3:c.1225C>T, XM_005269883.3:c.1225C>G, XM_005269883.2:c.1225C>T, XM_005269883.2:c.1225C>G, XM_005269883.1:c.1225C>T, XM_005269883.1:c.1225C>G, XM_011539855.3:c.568C>T, XM_011539855.3:c.568C>G, XM_011539855.2:c.568C>T, XM_011539855.2:c.568C>G, XM_011539855.1:c.568C>T, XM_011539855.1:c.568C>G, NM_001007274.1:c.*734C>T, NM_001007274.1:c.*734C>G, NM_001007275.1:c.*630C>T, NM_001007275.1:c.*630C>G, XM_047425305.1:c.568C>T, XM_047425305.1:c.568C>G, XM_047425308.1:c.568C>T, XM_047425308.1:c.568C>G, XM_047425306.1:c.568C>T, XM_047425306.1:c.568C>G, NP_057448.3:p.Arg190Ter, NP_057448.3:p.Arg190Gly, NP_001307771.1:p.Arg283Ter, NP_001307771.1:p.Arg283Gly, NP_001350443.1:p.Arg326Ter, NP_001350443.1:p.Arg326Gly, NP_001007274.1:p.Arg283Ter, NP_001007274.1:p.Arg283Gly, NP_001307772.1:p.Arg190Ter, NP_001307772.1:p.Arg190Gly, NP_001007273.1:p.Arg240Ter, NP_001007273.1:p.Arg240Gly, XP_005269940.1:p.Arg409Ter, XP_005269940.1:p.Arg409Gly, XP_011538157.1:p.Arg190Ter, XP_011538157.1:p.Arg190Gly, XP_047281261.1:p.Arg190Ter, XP_047281261.1:p.Arg190Gly, XP_047281264.1:p.Arg190Ter, XP_047281264.1:p.Arg190Gly, XP_047281262.1:p.Arg190Ter, XP_047281262.1:p.Arg190Gly

                              15.

                              rs2894246 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                C>T [Show Flanks]
                                Chromosome:
                                10:75095963 (GRCh38)
                                10:76855721 (GRCh37)
                                Canonical SPDI:
                                NC_000010.11:75095962:C:T
                                Gene:
                                DUSP13 (Varview)
                                Functional Consequence:
                                genic_downstream_transcript_variant,intron_variant
                                Validated:
                                by frequency,by alfa,by cluster
                                MAF:
                                T=0.075812/2718 (ALFA)
                                T=0.046092/46 (GoNL)
                                T=0.047768/214 (Estonian)
                                T=0.05/2 (GENOME_DK)
                                T=0.05/30 (NorthernSweden)
                                T=0.052154/201 (ALSPAC)
                                T=0.054746/203 (TWINSUK)
                                T=0.088673/12429 (GnomAD)
                                T=0.102633/27166 (TOPMED)
                                T=0.12963/28 (Qatari)
                                T=0.139913/701 (1000Genomes)
                                T=0.140575/88 (Chileans)
                                T=0.180952/38 (Vietnamese)
                                T=0.188351/249 (HapMap)
                                T=0.293857/861 (KOREAN)
                                T=0.302948/555 (Korea1K)
                                T=0.310001/5196 (TOMMO)
                                C=0.388889/7 (Siberian)
                                C=0.443662/63 (SGDP_PRJ)
                                HGVS:

                                16.

                                rs3740313 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  G>A,C [Show Flanks]
                                  Chromosome:
                                  10:75099346 (GRCh38)
                                  10:76859104 (GRCh37)
                                  Canonical SPDI:
                                  NC_000010.11:75099345:G:A,NC_000010.11:75099345:G:C
                                  Gene:
                                  DUSP13 (Varview), SAMD8 (Varview)
                                  Functional Consequence:
                                  5_prime_UTR_variant,intron_variant,upstream_transcript_variant,downstream_transcript_variant,coding_sequence_variant,2KB_upstream_variant,genic_downstream_transcript_variant,missense_variant
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  A=0.037267/1061 (ALFA)
                                  A=0.044944/24 (MGP)
                                  A=0.04509/45 (GoNL)
                                  A=0.047768/214 (Estonian)
                                  A=0.05/2 (GENOME_DK)
                                  A=0.05/30 (NorthernSweden)
                                  A=0.052932/204 (ALSPAC)
                                  A=0.055016/204 (TWINSUK)
                                  A=0.062124/537 (GnomAD_exomes)
                                  A=0.097044/151 (ExAC)
                                  A=0.102305/27079 (TOPMED)
                                  A=0.12963/28 (Qatari)
                                  A=0.134969/44 (HapMap)
                                  A=0.139444/698 (1000Genomes)
                                  A=0.190476/40 (Vietnamese)
                                  A=0.295904/867 (KOREAN)
                                  A=0.304039/557 (Korea1K)
                                  A=0.308019/5162 (TOMMO)
                                  G=0.388889/7 (Siberian)
                                  G=0.443662/63 (SGDP_PRJ)
                                  HGVS:

                                  17.

                                  rs3740314 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    A>C,T [Show Flanks]
                                    Chromosome:
                                    10:75099248 (GRCh38)
                                    10:76859006 (GRCh37)
                                    Canonical SPDI:
                                    NC_000010.11:75099247:A:C,NC_000010.11:75099247:A:T
                                    Gene:
                                    DUSP13 (Varview), SAMD8 (Varview)
                                    Functional Consequence:
                                    intron_variant,upstream_transcript_variant,downstream_transcript_variant,coding_sequence_variant,2KB_upstream_variant,genic_downstream_transcript_variant,missense_variant
                                    Validated:
                                    by frequency,by alfa,by cluster
                                    MAF:
                                    C=0.027453/474 (ALFA)
                                    C=0.044944/24 (MGP)
                                    C=0.04509/45 (GoNL)
                                    C=0.047991/215 (Estonian)
                                    C=0.05/2 (GENOME_DK)
                                    C=0.05/30 (NorthernSweden)
                                    C=0.052673/203 (ALSPAC)
                                    C=0.054746/203 (TWINSUK)
                                    C=0.062225/538 (GnomAD_exomes)
                                    C=0.088237/12375 (GnomAD)
                                    C=0.097205/153 (ExAC)
                                    C=0.102312/27081 (TOPMED)
                                    C=0.12963/28 (Qatari)
                                    C=0.1396/699 (1000Genomes)
                                    C=0.174528/37 (Vietnamese)
                                    C=0.295222/865 (KOREAN)
                                    C=0.304039/557 (Korea1K)
                                    C=0.308904/5177 (TOMMO)
                                    A=0.388889/7 (Siberian)
                                    A=0.443662/63 (SGDP_PRJ)
                                    HGVS:

                                    18.

                                    rs3740315 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      A>G [Show Flanks]
                                      Chromosome:
                                      10:75097958 (GRCh38)
                                      10:76857716 (GRCh37)
                                      Canonical SPDI:
                                      NC_000010.11:75097957:A:G
                                      Gene:
                                      DUSP13 (Varview), SAMD8 (Varview)
                                      Functional Consequence:
                                      genic_downstream_transcript_variant,intron_variant,2KB_upstream_variant,upstream_transcript_variant
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      G=0.232211/8315 (ALFA)
                                      G=0.104869/56 (MGP)
                                      G=0.161667/97 (NorthernSweden)
                                      G=0.20685/767 (TWINSUK)
                                      G=0.208355/803 (ALSPAC)
                                      G=0.233467/233 (GoNL)
                                      G=0.257024/35989 (GnomAD)
                                      G=0.267101/70699 (TOPMED)
                                      G=0.267634/1199 (Estonian)
                                      G=0.273148/59 (Qatari)
                                      G=0.275/11 (GENOME_DK)
                                      G=0.293897/549 (HapMap)
                                      G=0.330106/1653 (1000Genomes)
                                      A=0.33908/118 (SGDP_PRJ)
                                      A=0.34434/73 (Vietnamese)
                                      A=0.423077/11 (Siberian)
                                      A=0.462799/1356 (KOREAN)
                                      A=0.468398/7850 (TOMMO)
                                      A=0.480349/880 (Korea1K)
                                      HGVS:

                                      19.

                                      rs3740316 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        G>A [Show Flanks]
                                        Chromosome:
                                        10:75095663 (GRCh38)
                                        10:76855421 (GRCh37)
                                        Canonical SPDI:
                                        NC_000010.11:75095662:G:A
                                        Gene:
                                        DUSP13 (Varview)
                                        Functional Consequence:
                                        synonymous_variant,coding_sequence_variant,genic_downstream_transcript_variant,3_prime_UTR_variant
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        A=0.163397/29399 (ALFA)
                                        A=0.05/2 (GENOME_DK)
                                        A=0.136273/136 (GoNL)
                                        A=0.143747/554 (ALSPAC)
                                        A=0.15/672 (Estonian)
                                        A=0.151025/560 (TWINSUK)
                                        A=0.153333/92 (NorthernSweden)
                                        A=0.177226/2305 (GoESP)
                                        A=0.17752/21547 (ExAC)
                                        A=0.17831/24987 (GnomAD)
                                        A=0.179158/45055 (GnomAD_exomes)
                                        A=0.181648/97 (MGP)
                                        A=0.188618/116 (Vietnamese)
                                        A=0.193181/51133 (TOPMED)
                                        A=0.211274/1058 (1000Genomes)
                                        A=0.264271/500 (HapMap)
                                        A=0.291667/63 (Qatari)
                                        A=0.331058/970 (KOREAN)
                                        A=0.337336/618 (Korea1K)
                                        A=0.35643/5974 (TOMMO)
                                        G=0.375/9 (Siberian)
                                        G=0.418269/87 (SGDP_PRJ)
                                        HGVS:

                                        20.

                                        rs3740317 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          G>A [Show Flanks]
                                          Chromosome:
                                          10:75095654 (GRCh38)
                                          10:76855412 (GRCh37)
                                          Canonical SPDI:
                                          NC_000010.11:75095653:G:A
                                          Gene:
                                          DUSP13 (Varview)
                                          Functional Consequence:
                                          synonymous_variant,coding_sequence_variant,genic_downstream_transcript_variant,3_prime_UTR_variant
                                          Validated:
                                          by frequency,by alfa,by cluster
                                          MAF:
                                          A=0.281042/49632 (ALFA)
                                          A=0.195/117 (NorthernSweden)
                                          A=0.257551/955 (TWINSUK)
                                          A=0.259471/1000 (ALSPAC)
                                          A=0.269663/144 (MGP)
                                          A=0.288616/1293 (Estonian)
                                          A=0.289579/289 (GoNL)
                                          G=0.29902/183 (Vietnamese)
                                          A=0.3/12 (GENOME_DK)
                                          A=0.318853/4147 (GoESP)
                                          G=0.319797/126 (SGDP_PRJ)
                                          A=0.337988/41023 (ExAC)
                                          A=0.341006/47749 (GnomAD)
                                          A=0.346087/87029 (GnomAD_exomes)
                                          A=0.351852/76 (Qatari)
                                          A=0.35392/93679 (TOPMED)
                                          A=0.400212/754 (HapMap)
                                          G=0.415017/1216 (KOREAN)
                                          G=0.420306/770 (Korea1K)
                                          A=0.421299/2110 (1000Genomes)
                                          G=0.4375/14 (Siberian)
                                          G=0.443945/7441 (TOMMO)
                                          HGVS:

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