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Items: 1 to 20 of 37

1.

rs2070776 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    A>G,T [Show Flanks]
    Chromosome:
    17:63930138 (GRCh38)
    17:62007498 (GRCh37)
    Canonical SPDI:
    NC_000017.11:63930137:A:G,NC_000017.11:63930137:A:T
    Gene:
    CD79B (Varview)
    Functional Consequence:
    synonymous_variant,intron_variant,coding_sequence_variant,stop_gained
    Clinical significance:
    benign
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    A=0.347758/77751 (ALFA)
    A=0.263889/57 (Qatari)
    A=0.296196/109 (SGDP_PRJ)
    A=0.34/17 (Siberian)
    A=0.340381/4427 (GoESP)
    A=0.343042/1272 (TWINSUK)
    A=0.34442/1543 (Estonian)
    A=0.352705/352 (GoNL)
    A=0.354437/1366 (ALSPAC)
    A=0.357143/30 (PRJEB36033)
    A=0.358043/50154 (GnomAD)
    A=0.367883/97375 (TOPMED)
    A=0.378333/227 (NorthernSweden)
    A=0.386243/730 (HapMap)
    A=0.404831/48923 (ExAC)
    A=0.405319/31897 (PAGE_STUDY)
    A=0.410771/103050 (GnomAD_exomes)
    G=0.421348/225 (MGP)
    A=0.430464/130 (FINRISK)
    G=0.431818/266 (Vietnamese)
    G=0.433081/343 (PRJEB37584)
    A=0.437851/2193 (1000Genomes)
    G=0.45/18 (GENOME_DK)
    G=0.451536/1323 (KOREAN)
    A=0.454415/947 (HGDP_Stanford)
    G=0.48312/8097 (TOMMO)
    ...more
    HGVS:
    2.

    rs3791675 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      C>G,T [Show Flanks]
      Chromosome:
      2:55884174 (GRCh38)
      2:56111309 (GRCh37)
      Canonical SPDI:
      NC_000002.12:55884173:C:G,NC_000002.12:55884173:C:T
      Gene:
      EFEMP1 (Varview)
      Functional Consequence:
      intron_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      T=0.260883/68272 (ALFA)
      T=0.142857/2 (PRJEB36033)
      T=0.2/8 (GENOME_DK)
      T=0.203354/28483 (GnomAD)
      T=0.210586/55740 (TOPMED)
      T=0.221162/17405 (PAGE_STUDY)
      T=0.222045/139 (Chileans)
      T=0.225728/837 (TWINSUK)
      C=0.225939/662 (KOREAN)
      T=0.23/138 (NorthernSweden)
      T=0.23015/887 (ALSPAC)
      C=0.241266/442 (Korea1K)
      T=0.242485/242 (GoNL)
      C=0.257838/4321 (TOMMO)
      C=0.271028/58 (Vietnamese)
      T=0.278125/1246 (Estonian)
      T=0.279357/1399 (1000Genomes)
      T=0.28254/534 (HapMap)
      T=0.287037/62 (Qatari)
      C=0.305556/11 (Siberian)
      C=0.319444/92 (SGDP_PRJ)
      T=0.359292/406 (Daghestan)
      ...more
      HGVS:
      3.

      rs2780226 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        C>G,T [Show Flanks]
        Chromosome:
        6:34231315 (GRCh38)
        6:34199092 (GRCh37)
        Canonical SPDI:
        NC_000006.12:34231314:C:G,NC_000006.12:34231314:C:T
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        C=0.101787/18879 (ALFA)
        C=0.051667/31 (NorthernSweden)
        C=0.07369/284 (ALSPAC)
        C=0.083333/6 (PRJEB36033)
        C=0.085221/316 (TWINSUK)
        C=0.09018/90 (GoNL)
        C=0.1/4 (GENOME_DK)
        C=0.102273/81 (PRJEB37584)
        C=0.107143/6 (Siberian)
        C=0.127358/27 (Vietnamese)
        C=0.136538/71 (SGDP_PRJ)
        C=0.15546/2606 (TOMMO)
        C=0.162457/476 (KOREAN)
        C=0.175926/38 (Qatari)
        C=0.181223/332 (Korea1K)
        C=0.207009/29011 (GnomAD)
        C=0.221845/1111 (1000Genomes)
        C=0.23217/61453 (TOPMED)
        C=0.242585/458 (HapMap)
        C=0.316112/24866 (PAGE_STUDY)
        ...more
        HGVS:
        4.

        rs2724475 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          T>A,C [Show Flanks]
          Chromosome:
          4:17944809 (GRCh38)
          4:17946432 (GRCh37)
          Canonical SPDI:
          NC_000004.12:17944808:T:A,NC_000004.12:17944808:T:C
          Gene:
          LCORL (Varview)
          Functional Consequence:
          intron_variant
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          T=0.274786/5399 (ALFA)
          T=0.143519/31 (Qatari)
          T=0.209544/101 (SGDP_PRJ)
          T=0.222222/4 (PRJEB36033)
          T=0.252232/1130 (Estonian)
          T=0.255579/985 (ALSPAC)
          T=0.261905/11 (Siberian)
          T=0.264293/980 (TWINSUK)
          T=0.278333/167 (NorthernSweden)
          T=0.278557/278 (GoNL)
          T=0.290362/40646 (GnomAD)
          T=0.296981/78608 (TOPMED)
          T=0.314647/1576 (1000Genomes)
          T=0.325/13 (GENOME_DK)
          T=0.335612/26412 (PAGE_STUDY)
          T=0.381818/126 (HapMap)
          T=0.384259/83 (Vietnamese)
          C=0.453057/830 (Korea1K)
          T=0.466667/364 (PRJEB37584)
          C=0.467918/1371 (KOREAN)
          T=0.490728/8225 (TOMMO)
          ...more
          HGVS:
          5.

          rs2665838 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            C>A,G,T [Show Flanks]
            Chromosome:
            17:63889105 (GRCh38)
            17:61966465 (GRCh37)
            Canonical SPDI:
            NC_000017.11:63889104:C:A,NC_000017.11:63889104:C:G,NC_000017.11:63889104:C:T
            Validated:
            by frequency,by alfa,by cluster
            MAF:
            T=0./0 (ALFA)
            G=0./0 (PRJEB36033)
            G=0.044412/744 (TOMMO)
            G=0.061321/13 (Vietnamese)
            G=0.064682/189 (KOREAN)
            G=0.065502/120 (Korea1K)
            G=0.193785/970 (1000Genomes)
            G=0.197531/64 (HapMap)
            G=0.215/129 (NorthernSweden)
            G=0.235687/62384 (TOPMED)
            G=0.269071/1037 (ALSPAC)
            G=0.281823/1045 (TWINSUK)
            G=0.299599/299 (GoNL)
            G=0.319444/69 (Qatari)
            C=0.405063/64 (SGDP_PRJ)
            ...more
            HGVS:
            6.

            rs2421992 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              C>T [Show Flanks]
              Chromosome:
              1:172272111 (GRCh38)
              1:172241251 (GRCh37)
              Canonical SPDI:
              NC_000001.11:172272110:C:T
              Gene:
              DNM3 (Varview)
              Functional Consequence:
              intron_variant,genic_downstream_transcript_variant
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              C=0.322149/62727 (ALFA)
              C=0.238839/107 (SGDP_PRJ)
              C=0.258482/1158 (Estonian)
              C=0.266667/160 (NorthernSweden)
              C=0.269231/14 (Siberian)
              C=0.28942/848 (KOREAN)
              C=0.293884/4926 (TOMMO)
              C=0.295515/224 (PRJEB37584)
              C=0.299127/548 (Korea1K)
              C=0.3/12 (GENOME_DK)
              C=0.3/63 (Vietnamese)
              C=0.300467/1158 (ALSPAC)
              C=0.300712/338 (HapMap)
              C=0.31041/1151 (TWINSUK)
              C=0.317635/317 (GoNL)
              C=0.333333/14 (PRJEB36033)
              C=0.357354/724 (HGDP_Stanford)
              C=0.374238/52320 (GnomAD)
              C=0.380581/100736 (TOPMED)
              C=0.410056/2054 (1000Genomes)
              C=0.444444/96 (Qatari)
              ...more
              HGVS:
              7.

              rs2353398 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                T>A,C [Show Flanks]
                Chromosome:
                4:144601606 (GRCh38)
                4:145522758 (GRCh37)
                Canonical SPDI:
                NC_000004.12:144601605:T:A,NC_000004.12:144601605:T:C
                Validated:
                by frequency,by alfa,by cluster
                MAF:
                A=0.489233/4862 (ALFA)
                T=0./0 (PRJEB36033)
                T=0.208333/105 (SGDP_PRJ)
                T=0.221086/3705 (TOMMO)
                T=0.236855/18640 (PAGE_STUDY)
                T=0.237976/1192 (1000Genomes)
                T=0.246725/452 (Korea1K)
                T=0.26/13 (Siberian)
                T=0.269467/789 (KOREAN)
                T=0.27439/90 (HapMap)
                T=0.290404/230 (PRJEB37584)
                T=0.337448/89319 (TOPMED)
                T=0.337963/73 (Qatari)
                T=0.345094/47605 (GnomAD)
                T=0.410451/1838 (Estonian)
                T=0.435/261 (NorthernSweden)
                T=0.460922/460 (GoNL)
                A=0.475/19 (GENOME_DK)
                T=0.486785/1805 (TWINSUK)
                T=0.489362/1886 (ALSPAC)
                ...more
                HGVS:
                8.

                rs2280470 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  A>G [Show Flanks]
                  Chromosome:
                  15:88852395 (GRCh38)
                  15:89395626 (GRCh37)
                  Canonical SPDI:
                  NC_000015.10:88852394:A:G
                  Gene:
                  ACAN (Varview)
                  Functional Consequence:
                  intron_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  A=0.326584/11759 (ALFA)
                  G=0.179181/525 (KOREAN)
                  A=0.225/9 (GENOME_DK)
                  G=0.229953/3854 (TOMMO)
                  G=0.244216/190 (PRJEB37584)
                  G=0.259434/55 (Vietnamese)
                  A=0.2675/107 (SGDP_PRJ)
                  A=0.273148/59 (Qatari)
                  A=0.294118/10 (Siberian)
                  A=0.30151/1118 (TWINSUK)
                  A=0.314541/44025 (GnomAD)
                  A=0.316814/1221 (ALSPAC)
                  A=0.33081/87562 (TOPMED)
                  A=0.336673/336 (GoNL)
                  A=0.34/204 (NorthernSweden)
                  A=0.371652/1665 (Estonian)
                  A=0.375/30 (PRJEB36033)
                  A=0.38953/30656 (PAGE_STUDY)
                  A=0.392638/128 (HapMap)
                  A=0.412867/2068 (1000Genomes)
                  ...more
                  HGVS:
                  9.

                  rs2256183 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    A>G,T [Show Flanks]
                    Chromosome:
                    6:31412752 (GRCh38)
                    6:31380529 (GRCh37)
                    Canonical SPDI:
                    NC_000006.12:31412751:A:G,NC_000006.12:31412751:A:T
                    Gene:
                    MICA (Varview)
                    Functional Consequence:
                    intron_variant
                    Validated:
                    by frequency,by alfa,by cluster
                    MAF:
                    A=0.418619/40272 (ALFA)
                    A=0.140176/2347 (TOMMO)
                    A=0.166667/488 (KOREAN)
                    A=0.166667/8 (Siberian)
                    A=0.17619/37 (Vietnamese)
                    A=0.177122/96 (SGDP_PRJ)
                    A=0.208333/45 (Qatari)
                    A=0.221519/175 (PRJEB37584)
                    A=0.252655/1265 (1000Genomes)
                    A=0.259259/14 (PRJEB36033)
                    A=0.309091/102 (HapMap)
                    A=0.342023/90530 (TOPMED)
                    A=0.367972/51335 (GnomAD)
                    A=0.45/18 (GENOME_DK)
                    G=0.468333/281 (NorthernSweden)
                    A=0.476954/476 (GoNL)
                    G=0.494032/1904 (ALSPAC)
                    G=0.495955/1839 (TWINSUK)
                    ...more
                    HGVS:
                    10.

                    rs2145998 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      T>A,G [Show Flanks]
                      Chromosome:
                      10:79361940 (GRCh38)
                      10:81121696 (GRCh37)
                      Canonical SPDI:
                      NC_000010.11:79361939:T:A,NC_000010.11:79361939:T:G
                      Validated:
                      by frequency,by alfa,by cluster
                      MAF:
                      A=0.47979/8689 (ALFA)
                      T=0.285714/12 (Siberian)
                      T=0.296875/133 (SGDP_PRJ)
                      T=0.313652/919 (KOREAN)
                      T=0.325472/69 (Vietnamese)
                      T=0.336852/5646 (TOMMO)
                      T=0.394737/30 (PRJEB36033)
                      A=0.457447/1763 (ALSPAC)
                      T=0.459375/2058 (Estonian)
                      T=0.463333/278 (NorthernSweden)
                      A=0.472946/472 (GoNL)
                      T=0.475/19 (GENOME_DK)
                      A=0.476268/1766 (TWINSUK)
                      T=0.479197/37708 (PAGE_STUDY)
                      A=0.48355/67344 (GnomAD)
                      A=0.485436/128490 (TOPMED)
                      A=0.486111/105 (Qatari)
                      T=0.490798/160 (HapMap)
                      T=0.498438/2496 (1000Genomes)
                      ...more
                      HGVS:
                      11.

                      rs3792752 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        A>G [Show Flanks]
                        Chromosome:
                        5:32768528 (GRCh38)
                        5:32768634 (GRCh37)
                        Canonical SPDI:
                        NC_000005.10:32768527:A:G
                        Gene:
                        NPR3 (Varview)
                        Functional Consequence:
                        intron_variant
                        Validated:
                        by frequency,by alfa,by cluster
                        MAF:
                        G=0.268023/69195 (ALFA)
                        G=0.154206/33 (Vietnamese)
                        G=0.160354/127 (PRJEB37584)
                        G=0.190444/558 (KOREAN)
                        G=0.203704/44 (Qatari)
                        G=0.22245/3728 (TOMMO)
                        G=0.228764/474 (HGDP_Stanford)
                        G=0.258173/995 (ALSPAC)
                        G=0.259709/963 (TWINSUK)
                        G=0.275/11 (GENOME_DK)
                        G=0.275/165 (NorthernSweden)
                        G=0.282565/282 (GoNL)
                        G=0.299107/1340 (Estonian)
                        G=0.305278/1529 (1000Genomes)
                        G=0.314107/43970 (GnomAD)
                        G=0.316993/83905 (TOPMED)
                        G=0.318326/601 (HapMap)
                        G=0.334263/26253 (PAGE_STUDY)
                        G=0.361111/26 (PRJEB36033)
                        A=0.444444/112 (SGDP_PRJ)
                        A=0.458333/11 (Siberian)
                        ...more
                        HGVS:
                        12.

                        rs1401796 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          C>A,G,T [Show Flanks]
                          Chromosome:
                          17:56762398 (GRCh38)
                          17:54839759 (GRCh37)
                          Canonical SPDI:
                          NC_000017.11:56762397:C:A,NC_000017.11:56762397:C:G,NC_000017.11:56762397:C:T
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          C=0.464605/11656 (ALFA)
                          T=0./0 (KOREAN)
                          C=0.08679/159 (Korea1K)
                          C=0.116822/25 (Vietnamese)
                          C=0.162786/2728 (TOMMO)
                          C=0.204545/9 (Siberian)
                          C=0.24359/114 (SGDP_PRJ)
                          C=0.27907/24 (PRJEB36033)
                          C=0.378568/29788 (PAGE_STUDY)
                          C=0.386165/1934 (1000Genomes)
                          C=0.387473/730 (HapMap)
                          C=0.438725/116126 (TOPMED)
                          A=0.45/18 (GENOME_DK)
                          C=0.458233/64149 (GnomAD)
                          A=0.46994/469 (GoNL)
                          C=0.47068/1814 (ALSPAC)
                          A=0.476852/103 (Qatari)
                          C=0.481661/1786 (TWINSUK)
                          A=0.483482/2166 (Estonian)
                          C=0.496667/298 (NorthernSweden)
                          ...more
                          HGVS:
                          13.

                          rs1367226 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            A>C,G,T [Show Flanks]
                            Chromosome:
                            2:55862405 (GRCh38)
                            2:56089540 (GRCh37)
                            Canonical SPDI:
                            NC_000002.12:55862404:A:C,NC_000002.12:55862404:A:G,NC_000002.12:55862404:A:T
                            Gene:
                            LOC112268416 (Varview)
                            Functional Consequence:
                            intron_variant
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            A=0.384509/26778 (ALFA)
                            T=0./0 (KOREAN)
                            A=0.090909/72 (PRJEB37584)
                            A=0.105349/193 (Korea1K)
                            A=0.135855/2277 (TOMMO)
                            A=0.138095/29 (Vietnamese)
                            A=0.173913/8 (Siberian)
                            A=0.186235/92 (SGDP_PRJ)
                            A=0.19556/370 (HapMap)
                            A=0.270144/1353 (1000Genomes)
                            A=0.280268/22056 (PAGE_STUDY)
                            A=0.287037/62 (Qatari)
                            A=0.32821/86874 (TOPMED)
                            A=0.343428/48073 (GnomAD)
                            G=0.420128/263 (Chileans)
                            A=0.432278/1666 (ALSPAC)
                            A=0.436624/1619 (TWINSUK)
                            A=0.447896/447 (GoNL)
                            G=0.451667/271 (NorthernSweden)
                            G=0.484598/2171 (Estonian)
                            A=0.484848/32 (PRJEB36033)
                            A=0.5/20 (GENOME_DK)
                            ...more
                            HGVS:
                            14.

                            rs1173727 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              T>A,C,G [Show Flanks]
                              Chromosome:
                              5:32830415 (GRCh38)
                              5:32830521 (GRCh37)
                              Canonical SPDI:
                              NC_000005.10:32830414:T:A,NC_000005.10:32830414:T:C,NC_000005.10:32830414:T:G
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              T=0.396341/72937 (ALFA)
                              G=0./0 (KOREAN)
                              T=0.217949/102 (SGDP_PRJ)
                              T=0.23913/11 (Siberian)
                              T=0.311461/24512 (PAGE_STUDY)
                              T=0.319444/253 (PRJEB37584)
                              T=0.341724/90451 (TOPMED)
                              T=0.343042/48052 (GnomAD)
                              T=0.345565/1731 (1000Genomes)
                              T=0.352761/115 (HapMap)
                              T=0.35514/76 (Vietnamese)
                              T=0.39083/716 (Korea1K)
                              T=0.394822/1464 (TWINSUK)
                              T=0.398148/86 (Qatari)
                              T=0.398333/239 (NorthernSweden)
                              T=0.401804/401 (GoNL)
                              T=0.406823/6818 (TOMMO)
                              T=0.415413/1601 (ALSPAC)
                              T=0.421053/32 (PRJEB36033)
                              T=0.430804/1930 (Estonian)
                              T=0.45/18 (GENOME_DK)
                              ...more
                              HGVS:
                              15.

                              rs879882 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                T>C,G [Show Flanks]
                                Chromosome:
                                6:31171675 (GRCh38)
                                6:31139452 (GRCh37)
                                Canonical SPDI:
                                NC_000006.12:31171674:T:C,NC_000006.12:31171674:T:G
                                Gene:
                                POU5F1 (Varview)
                                Functional Consequence:
                                upstream_transcript_variant,2KB_upstream_variant
                                Validated:
                                by frequency,by alfa,by cluster
                                MAF:
                                T=0.366751/52086 (ALFA)
                                C=0.009615/2 (Korea1K)
                                T=0.289474/11 (GENOME_DK)
                                T=0.3/15 (Siberian)
                                T=0.300885/136 (SGDP_PRJ)
                                T=0.305556/22 (PRJEB36033)
                                T=0.337963/73 (Qatari)
                                T=0.344837/1329 (ALSPAC)
                                T=0.352211/1306 (TWINSUK)
                                T=0.367839/75435 (GENOGRAPHIC)
                                T=0.371667/223 (NorthernSweden)
                                T=0.38849/53349 (GnomAD)
                                T=0.395508/104687 (TOPMED)
                                T=0.401562/1799 (Estonian)
                                C=0.411925/6888 (TOMMO)
                                T=0.423151/881 (HGDP_Stanford)
                                T=0.440974/2208 (1000Genomes)
                                T=0.440982/34595 (PAGE_STUDY)
                                T=0.464513/877 (HapMap)
                                C=0.464646/368 (PRJEB37584)
                                C=0.472317/1382 (KOREAN)
                                ...more
                                HGVS:
                                16.

                                rs750460 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  G>A,C,T [Show Flanks]
                                  Chromosome:
                                  15:73949165 (GRCh38)
                                  15:74241506 (GRCh37)
                                  Canonical SPDI:
                                  NC_000015.10:73949164:G:A,NC_000015.10:73949164:G:C,NC_000015.10:73949164:G:T
                                  Gene:
                                  LOXL1 (Varview)
                                  Functional Consequence:
                                  intron_variant,genic_downstream_transcript_variant
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  T=0./0 (ALFA)
                                  A=0.060185/13 (Vietnamese)
                                  A=0.087031/255 (KOREAN)
                                  A=0.090909/72 (PRJEB37584)
                                  A=0.102626/1720 (TOMMO)
                                  A=0.224242/74 (HapMap)
                                  A=0.2703/1354 (1000Genomes)
                                  A=0.270839/21315 (PAGE_STUDY)
                                  A=0.282609/26 (PRJEB36033)
                                  A=0.360871/95519 (TOPMED)
                                  G=0.374016/95 (SGDP_PRJ)
                                  A=0.37963/82 (Qatari)
                                  G=0.392857/11 (Siberian)
                                  G=0.4/16 (GENOME_DK)
                                  A=0.451667/271 (NorthernSweden)
                                  A=0.45992/459 (GoNL)
                                  A=0.466269/1797 (ALSPAC)
                                  A=0.478425/1774 (TWINSUK)
                                  G=0.498214/2232 (Estonian)
                                  ...more
                                  HGVS:
                                  17.

                                  rs572169 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    C>T [Show Flanks]
                                    Chromosome:
                                    3:172447937 (GRCh38)
                                    3:172165727 (GRCh37)
                                    Canonical SPDI:
                                    NC_000003.12:172447936:C:T
                                    Gene:
                                    GHSR (Varview)
                                    Functional Consequence:
                                    coding_sequence_variant,synonymous_variant
                                    Clinical significance:
                                    benign
                                    Validated:
                                    by frequency,by alfa,by cluster
                                    MAF:
                                    T=0.295048/106009 (ALFA)
                                    T=0.02381/2 (PRJEB36033)
                                    T=0.111111/24 (Qatari)
                                    T=0.136704/73 (MGP)
                                    T=0.175/7 (GENOME_DK)
                                    T=0.201205/334 (HapMap)
                                    T=0.230586/2999 (GoESP)
                                    T=0.232511/1164 (1000Genomes)
                                    T=0.233471/18327 (PAGE_STUDY)
                                    T=0.244986/34322 (GnomAD)
                                    T=0.245147/64888 (TOPMED)
                                    T=0.296205/1327 (Estonian)
                                    T=0.301768/36386 (ExAC)
                                    T=0.305662/637 (HGDP_Stanford)
                                    T=0.307829/77121 (GnomAD_exomes)
                                    T=0.309187/350 (Daghestan)
                                    T=0.309331/1147 (TWINSUK)
                                    T=0.311258/94 (FINRISK)
                                    T=0.315257/1215 (ALSPAC)
                                    T=0.327778/177 (Vietnamese)
                                    T=0.335671/335 (GoNL)
                                    C=0.361111/104 (SGDP_PRJ)
                                    T=0.378333/227 (NorthernSweden)
                                    C=0.388889/14 (Siberian)
                                    T=0.412166/6908 (TOMMO)
                                    T=0.45321/1327 (KOREAN)
                                    T=0.467249/856 (Korea1K)
                                    T=0.480964/379 (PRJEB37584)
                                    ...more
                                    HGVS:
                                    18.

                                    rs227724 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      A>C,T [Show Flanks]
                                      Chromosome:
                                      17:56701456 (GRCh38)
                                      17:54778817 (GRCh37)
                                      Canonical SPDI:
                                      NC_000017.11:56701455:A:C,NC_000017.11:56701455:A:T
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      T=0.321651/26928 (ALFA)
                                      T=0.157895/12 (PRJEB36033)
                                      T=0.251163/19759 (PAGE_STUDY)
                                      T=0.252538/199 (PRJEB37584)
                                      T=0.269966/791 (KOREAN)
                                      T=0.274364/518 (HapMap)
                                      T=0.275/11 (GENOME_DK)
                                      T=0.288277/76304 (TOPMED)
                                      T=0.289819/1451 (1000Genomes)
                                      T=0.300926/65 (Vietnamese)
                                      T=0.303666/5089 (TOMMO)
                                      T=0.306361/42901 (GnomAD)
                                      T=0.324338/1250 (ALSPAC)
                                      T=0.333333/72 (Qatari)
                                      T=0.343042/1272 (TWINSUK)
                                      T=0.347695/347 (GoNL)
                                      T=0.353333/212 (NorthernSweden)
                                      T=0.36942/1655 (Estonian)
                                      A=0.382353/13 (Siberian)
                                      A=0.387597/100 (SGDP_PRJ)
                                      ...more
                                      HGVS:
                                      19.

                                      rs225694 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        A>C,G,T [Show Flanks]
                                        Chromosome:
                                        6:142206005 (GRCh38)
                                        6:142527142 (GRCh37)
                                        Canonical SPDI:
                                        NC_000006.12:142206004:A:C,NC_000006.12:142206004:A:G,NC_000006.12:142206004:A:T
                                        Gene:
                                        VTA1 (Varview)
                                        Functional Consequence:
                                        intron_variant
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        A=0.196784/3831 (ALFA)
                                        T=0./0 (KOREAN)
                                        A=0./0 (PRJEB36033)
                                        A=0.022295/374 (TOMMO)
                                        A=0.031646/25 (PRJEB37584)
                                        A=0.038095/8 (Vietnamese)
                                        A=0.053571/3 (Siberian)
                                        A=0.073171/24 (HapMap)
                                        A=0.105556/57 (SGDP_PRJ)
                                        A=0.125/5 (GENOME_DK)
                                        A=0.137883/691 (1000Genomes)
                                        A=0.160554/42497 (TOPMED)
                                        A=0.162894/22829 (GnomAD)
                                        A=0.185185/40 (Qatari)
                                        A=0.191667/115 (NorthernSweden)
                                        A=0.225221/868 (ALSPAC)
                                        A=0.226786/1016 (Estonian)
                                        A=0.229504/851 (TWINSUK)
                                        A=0.231463/231 (GoNL)
                                        ...more
                                        HGVS:
                                        20.

                                        rs7763064 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          G>A,T [Show Flanks]
                                          Chromosome:
                                          6:142476152 (GRCh38)
                                          6:142797289 (GRCh37)
                                          Canonical SPDI:
                                          NC_000006.12:142476151:G:A,NC_000006.12:142476151:G:T
                                          Validated:
                                          by frequency,by alfa,by cluster
                                          MAF:
                                          A=0.320274/61991 (ALFA)
                                          A=0.246667/148 (NorthernSweden)
                                          A=0.261523/261 (GoNL)
                                          A=0.281785/1086 (ALSPAC)
                                          A=0.289374/1073 (TWINSUK)
                                          A=0.30303/20 (PRJEB36033)
                                          A=0.303125/1358 (Estonian)
                                          A=0.305128/238 (PRJEB37584)
                                          A=0.327476/205 (Chileans)
                                          A=0.331399/971 (KOREAN)
                                          G=0.349432/123 (SGDP_PRJ)
                                          A=0.351852/399 (Daghestan)
                                          A=0.361354/662 (Korea1K)
                                          A=0.375/15 (GENOME_DK)
                                          A=0.385188/53907 (GnomAD)
                                          A=0.38785/83 (Vietnamese)
                                          A=0.393056/104038 (TOPMED)
                                          A=0.407407/88 (Qatari)
                                          A=0.414741/2077 (1000Genomes)
                                          A=0.44298/34859 (PAGE_STUDY)
                                          A=0.468783/886 (HapMap)
                                          G=0.5/13 (Siberian)
                                          ...more
                                          HGVS:

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