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Items: 4

1.

rs1041983 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    C>T [Show Flanks]
    Chromosome:
    8:18400285 (GRCh38)
    8:18257795 (GRCh37)
    Gene:
    NAT2 (Varview)
    Functional Consequence:
    coding_sequence_variant,synonymous_variant
    Clinical significance:
    drug-response
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    T=0.32583/41426 (ALFA)
    T=0.282895/86 (FINRISK)
    T=0.288333/173 (NorthernSweden)
    T=0.300926/65 (Qatari)
    T=0.302605/302 (GoNL)
    T=0.307116/164 (MGP)
    T=0.3125/1400 (Estonian)
    T=0.314995/1168 (TWINSUK)
    T=0.322782/1244 (ALSPAC)
    T=0.328669/963 (KOREAN)
    T=0.341977/85599 (GnomAD_exomes)
    T=0.34489/41762 (ExAC)
    T=0.356253/11150 (GnomAD)
    T=0.357374/4648 (GoESP)
    T=0.363604/45657 (TOPMED)
    C=0.369697/122 (SGDP_PRJ)
    T=0.375/15 (GENOME_DK)
    T=0.390244/736 (HapMap)
    T=0.397364/1990 (1000Genomes)
    C=0.464286/13 (Siberian)
    T=0.493377/298 (Vietnamese)
    HGVS:
    NC_000008.11:g.18400285C>T, NC_000008.10:g.18257795C>T, NG_012246.1:g.14041C>T, NM_000015.3:c.282C>T, NM_000015.2:c.282C>T, XM_017012938.1:c.282C>T
    2.

    rs59855457 has merged into rs1041983 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      C>T [Show Flanks]
      Chromosome:
      8:18400285 (GRCh38)
      8:18257795 (GRCh37)
      Gene:
      NAT2 (Varview)
      Functional Consequence:
      coding_sequence_variant,synonymous_variant
      Clinical significance:
      drug-response
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      T=0.32583/41426 (ALFA)
      T=0.282895/86 (FINRISK)
      T=0.288333/173 (NorthernSweden)
      T=0.300926/65 (Qatari)
      T=0.302605/302 (GoNL)
      T=0.307116/164 (MGP)
      T=0.3125/1400 (Estonian)
      T=0.314995/1168 (TWINSUK)
      T=0.322782/1244 (ALSPAC)
      T=0.328669/963 (KOREAN)
      T=0.341977/85599 (GnomAD_exomes)
      T=0.34489/41762 (ExAC)
      T=0.356253/11150 (GnomAD)
      T=0.357374/4648 (GoESP)
      T=0.363604/45657 (TOPMED)
      C=0.369697/122 (SGDP_PRJ)
      T=0.375/15 (GENOME_DK)
      T=0.390244/736 (HapMap)
      T=0.397364/1990 (1000Genomes)
      C=0.464286/13 (Siberian)
      T=0.493377/298 (Vietnamese)
      HGVS:
      NC_000008.11:g.18400285C>T, NC_000008.10:g.18257795C>T, NG_012246.1:g.14041C>T, NM_000015.3:c.282C>T, NM_000015.2:c.282C>T, XM_017012938.1:c.282C>T
      3.

      rs17858364 has merged into rs1041983 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        C>T [Show Flanks]
        Chromosome:
        8:18400285 (GRCh38)
        8:18257795 (GRCh37)
        Gene:
        NAT2 (Varview)
        Functional Consequence:
        coding_sequence_variant,synonymous_variant
        Clinical significance:
        drug-response
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        T=0.32583/41426 (ALFA)
        T=0.282895/86 (FINRISK)
        T=0.288333/173 (NorthernSweden)
        T=0.300926/65 (Qatari)
        T=0.302605/302 (GoNL)
        T=0.307116/164 (MGP)
        T=0.3125/1400 (Estonian)
        T=0.314995/1168 (TWINSUK)
        T=0.322782/1244 (ALSPAC)
        T=0.328669/963 (KOREAN)
        T=0.341977/85599 (GnomAD_exomes)
        T=0.34489/41762 (ExAC)
        T=0.356253/11150 (GnomAD)
        T=0.357374/4648 (GoESP)
        T=0.363604/45657 (TOPMED)
        C=0.369697/122 (SGDP_PRJ)
        T=0.375/15 (GENOME_DK)
        T=0.390244/736 (HapMap)
        T=0.397364/1990 (1000Genomes)
        C=0.464286/13 (Siberian)
        T=0.493377/298 (Vietnamese)
        HGVS:
        NC_000008.11:g.18400285C>T, NC_000008.10:g.18257795C>T, NG_012246.1:g.14041C>T, NM_000015.3:c.282C>T, NM_000015.2:c.282C>T, XM_017012938.1:c.282C>T
        4.

        rs17845484 has merged into rs1041983 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          C>T [Show Flanks]
          Chromosome:
          8:18400285 (GRCh38)
          8:18257795 (GRCh37)
          Gene:
          NAT2 (Varview)
          Functional Consequence:
          coding_sequence_variant,synonymous_variant
          Clinical significance:
          drug-response
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          T=0.32583/41426 (ALFA)
          T=0.282895/86 (FINRISK)
          T=0.288333/173 (NorthernSweden)
          T=0.300926/65 (Qatari)
          T=0.302605/302 (GoNL)
          T=0.307116/164 (MGP)
          T=0.3125/1400 (Estonian)
          T=0.314995/1168 (TWINSUK)
          T=0.322782/1244 (ALSPAC)
          T=0.328669/963 (KOREAN)
          T=0.341977/85599 (GnomAD_exomes)
          T=0.34489/41762 (ExAC)
          T=0.356253/11150 (GnomAD)
          T=0.357374/4648 (GoESP)
          T=0.363604/45657 (TOPMED)
          C=0.369697/122 (SGDP_PRJ)
          T=0.375/15 (GENOME_DK)
          T=0.390244/736 (HapMap)
          T=0.397364/1990 (1000Genomes)
          C=0.464286/13 (Siberian)
          T=0.493377/298 (Vietnamese)
          HGVS:
          NC_000008.11:g.18400285C>T, NC_000008.10:g.18257795C>T, NG_012246.1:g.14041C>T, NM_000015.3:c.282C>T, NM_000015.2:c.282C>T, XM_017012938.1:c.282C>T

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