Display Settings:

Format
Sort by

Send to:

Choose Destination

Search results

Items: 5

1.

rs1799929 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    C>T [Show Flanks]
    Chromosome:
    8:18400484 (GRCh38)
    8:18257994 (GRCh37)
    Gene:
    NAT2 (Varview)
    Functional Consequence:
    coding_sequence_variant,synonymous_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    T=0.416553/80898 (ALFA)
    T=0.019105/35 (Korea1K)
    T=0.020534/60 (KOREAN)
    T=0.066558/41 (Vietnamese)
    T=0.26542/20888 (PAGE_STUDY)
    T=0.267971/1342 (1000Genomes)
    T=0.278252/522 (HapMap)
    T=0.341385/42867 (TOPMED)
    T=0.359425/225 (Chileans)
    T=0.361228/11305 (GnomAD)
    T=0.361278/90469 (GnomAD_exomes)
    T=0.364034/44062 (ExAC)
    T=0.370983/4825 (GoESP)
    C=0.386364/17 (Siberian)
    C=0.389344/95 (SGDP_PRJ)
    T=0.425/17 (GENOME_DK)
    T=0.425013/1638 (ALSPAC)
    T=0.434196/1610 (TWINSUK)
    T=0.440882/440 (GoNL)
    T=0.444643/1992 (Estonian)
    T=0.445693/238 (MGP)
    T=0.447368/136 (FINRISK)
    T=0.453704/98 (Qatari)
    T=0.468333/281 (NorthernSweden)
    HGVS:
    NC_000008.11:g.18400484C>T, NC_000008.10:g.18257994C>T, NG_012246.1:g.14240C>T, NM_000015.3:c.481C>T, NM_000015.2:c.481C>T, XM_017012938.1:c.481C>T
    2.

    rs60310310 has merged into rs1799929 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      C>T [Show Flanks]
      Chromosome:
      8:18400484 (GRCh38)
      8:18257994 (GRCh37)
      Gene:
      NAT2 (Varview)
      Functional Consequence:
      coding_sequence_variant,synonymous_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      T=0.416553/80898 (ALFA)
      T=0.019105/35 (Korea1K)
      T=0.020534/60 (KOREAN)
      T=0.066558/41 (Vietnamese)
      T=0.26542/20888 (PAGE_STUDY)
      T=0.267971/1342 (1000Genomes)
      T=0.278252/522 (HapMap)
      T=0.341385/42867 (TOPMED)
      T=0.359425/225 (Chileans)
      T=0.361228/11305 (GnomAD)
      T=0.361278/90469 (GnomAD_exomes)
      T=0.364034/44062 (ExAC)
      T=0.370983/4825 (GoESP)
      C=0.386364/17 (Siberian)
      C=0.389344/95 (SGDP_PRJ)
      T=0.425/17 (GENOME_DK)
      T=0.425013/1638 (ALSPAC)
      T=0.434196/1610 (TWINSUK)
      T=0.440882/440 (GoNL)
      T=0.444643/1992 (Estonian)
      T=0.445693/238 (MGP)
      T=0.447368/136 (FINRISK)
      T=0.453704/98 (Qatari)
      T=0.468333/281 (NorthernSweden)
      HGVS:
      NC_000008.11:g.18400484C>T, NC_000008.10:g.18257994C>T, NG_012246.1:g.14240C>T, NM_000015.3:c.481C>T, NM_000015.2:c.481C>T, XM_017012938.1:c.481C>T
      3.

      rs58882350 has merged into rs1799929 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        C>T [Show Flanks]
        Chromosome:
        8:18400484 (GRCh38)
        8:18257994 (GRCh37)
        Gene:
        NAT2 (Varview)
        Functional Consequence:
        coding_sequence_variant,synonymous_variant
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        T=0.416553/80898 (ALFA)
        T=0.019105/35 (Korea1K)
        T=0.020534/60 (KOREAN)
        T=0.066558/41 (Vietnamese)
        T=0.26542/20888 (PAGE_STUDY)
        T=0.267971/1342 (1000Genomes)
        T=0.278252/522 (HapMap)
        T=0.341385/42867 (TOPMED)
        T=0.359425/225 (Chileans)
        T=0.361228/11305 (GnomAD)
        T=0.361278/90469 (GnomAD_exomes)
        T=0.364034/44062 (ExAC)
        T=0.370983/4825 (GoESP)
        C=0.386364/17 (Siberian)
        C=0.389344/95 (SGDP_PRJ)
        T=0.425/17 (GENOME_DK)
        T=0.425013/1638 (ALSPAC)
        T=0.434196/1610 (TWINSUK)
        T=0.440882/440 (GoNL)
        T=0.444643/1992 (Estonian)
        T=0.445693/238 (MGP)
        T=0.447368/136 (FINRISK)
        T=0.453704/98 (Qatari)
        T=0.468333/281 (NorthernSweden)
        HGVS:
        NC_000008.11:g.18400484C>T, NC_000008.10:g.18257994C>T, NG_012246.1:g.14240C>T, NM_000015.3:c.481C>T, NM_000015.2:c.481C>T, XM_017012938.1:c.481C>T
        4.

        rs17595342 has merged into rs1799929 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          C>T [Show Flanks]
          Chromosome:
          8:18400484 (GRCh38)
          8:18257994 (GRCh37)
          Gene:
          NAT2 (Varview)
          Functional Consequence:
          coding_sequence_variant,synonymous_variant
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          T=0.416553/80898 (ALFA)
          T=0.019105/35 (Korea1K)
          T=0.020534/60 (KOREAN)
          T=0.066558/41 (Vietnamese)
          T=0.26542/20888 (PAGE_STUDY)
          T=0.267971/1342 (1000Genomes)
          T=0.278252/522 (HapMap)
          T=0.341385/42867 (TOPMED)
          T=0.359425/225 (Chileans)
          T=0.361228/11305 (GnomAD)
          T=0.361278/90469 (GnomAD_exomes)
          T=0.364034/44062 (ExAC)
          T=0.370983/4825 (GoESP)
          C=0.386364/17 (Siberian)
          C=0.389344/95 (SGDP_PRJ)
          T=0.425/17 (GENOME_DK)
          T=0.425013/1638 (ALSPAC)
          T=0.434196/1610 (TWINSUK)
          T=0.440882/440 (GoNL)
          T=0.444643/1992 (Estonian)
          T=0.445693/238 (MGP)
          T=0.447368/136 (FINRISK)
          T=0.453704/98 (Qatari)
          T=0.468333/281 (NorthernSweden)
          HGVS:
          NC_000008.11:g.18400484C>T, NC_000008.10:g.18257994C>T, NG_012246.1:g.14240C>T, NM_000015.3:c.481C>T, NM_000015.2:c.481C>T, XM_017012938.1:c.481C>T
          5.

          rs4646268 has merged into rs1799929 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            C>T [Show Flanks]
            Chromosome:
            8:18400484 (GRCh38)
            8:18257994 (GRCh37)
            Gene:
            NAT2 (Varview)
            Functional Consequence:
            coding_sequence_variant,synonymous_variant
            Validated:
            by frequency,by alfa,by cluster
            MAF:
            T=0.416553/80898 (ALFA)
            T=0.019105/35 (Korea1K)
            T=0.020534/60 (KOREAN)
            T=0.066558/41 (Vietnamese)
            T=0.26542/20888 (PAGE_STUDY)
            T=0.267971/1342 (1000Genomes)
            T=0.278252/522 (HapMap)
            T=0.341385/42867 (TOPMED)
            T=0.359425/225 (Chileans)
            T=0.361228/11305 (GnomAD)
            T=0.361278/90469 (GnomAD_exomes)
            T=0.364034/44062 (ExAC)
            T=0.370983/4825 (GoESP)
            C=0.386364/17 (Siberian)
            C=0.389344/95 (SGDP_PRJ)
            T=0.425/17 (GENOME_DK)
            T=0.425013/1638 (ALSPAC)
            T=0.434196/1610 (TWINSUK)
            T=0.440882/440 (GoNL)
            T=0.444643/1992 (Estonian)
            T=0.445693/238 (MGP)
            T=0.447368/136 (FINRISK)
            T=0.453704/98 (Qatari)
            T=0.468333/281 (NorthernSweden)
            HGVS:
            NC_000008.11:g.18400484C>T, NC_000008.10:g.18257994C>T, NG_012246.1:g.14240C>T, NM_000015.3:c.481C>T, NM_000015.2:c.481C>T, XM_017012938.1:c.481C>T

            Display Settings:

            Format
            Sort by

            Send to:

            Choose Destination

            Supplemental Content

            Find related data

            Search details

            See more...

            Recent activity

            Your browsing activity is empty.

            Activity recording is turned off.

            Turn recording back on

            See more...
            Support Center