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Items: 1 to 20 of 28462

1.

rs1491475481 has merged into rs72215351 [Homo sapiens]
    Variant type:
    DELINS
    Alleles:
    TA>-,TATA [Show Flanks]
    Chromosome:
    5:8411249 (GRCh38)
    5:8411362 (GRCh37)
    Canonical SPDI:
    NC_000005.10:8411247:ATA:A,NC_000005.10:8411247:ATA:ATATA
    Gene:
    LINC02226 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    A=0.097171/1587 (ALFA)
    -=0.003362/56 (TOMMO)
    -=0.009279/17 (Korea1K)
    -=0.083466/418 (1000Genomes)
    -=0.086384/387 (Estonian)
    -=0.092266/24422 (TOPMED)
    -=0.094006/13061 (GnomAD)
    -=0.115385/69 (NorthernSweden)
    -=0.125/5 (GENOME_DK)
    -=0.138038/532 (ALSPAC)
    -=0.148297/148 (GoNL)
    -=0.148598/551 (TWINSUK)
    ...more
    HGVS:
    2.

    rs1491470453 has merged into rs11370658 [Homo sapiens]
      Variant type:
      DELINS
      Alleles:
      TTTTTTTTT>-,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT [Show Flanks]
      Chromosome:
      5:8449471 (GRCh38)
      5:8449584 (GRCh37)
      Canonical SPDI:
      NC_000005.10:8449461:TTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000005.10:8449461:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000005.10:8449461:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000005.10:8449461:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000005.10:8449461:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000005.10:8449461:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000005.10:8449461:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000005.10:8449461:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000005.10:8449461:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000005.10:8449461:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000005.10:8449461:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:8449461:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:8449461:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:8449461:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT
      Gene:
      LINC02226 (Varview)
      Functional Consequence:
      intron_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      TTTTTTTTTTTT=0./0 (ALFA)
      -=0.000004/1 (TOPMED)
      HGVS:
      3.

      rs1491449615 [Homo sapiens]
        Variant type:
        INS
        Alleles:
        ->CA [Show Flanks]
        Chromosome:
        5:8419051 (GRCh38)
        5:8419165 (GRCh37)
        Canonical SPDI:
        NC_000005.10:8419051::CA
        Gene:
        LINC02226 (Varview)
        Functional Consequence:
        intron_variant
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        CA=0./0 (ALFA)
        CA=0.000018/2 (GnomAD)
        HGVS:
        4.

        rs1491402958 [Homo sapiens]
          Variant type:
          INS
          Alleles:
          ->C [Show Flanks]
          Chromosome:
          5:8449462 (GRCh38)
          5:8449576 (GRCh37)
          Canonical SPDI:
          NC_000005.10:8449462::C
          Gene:
          LINC02226 (Varview)
          Functional Consequence:
          intron_variant
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          C=0.000084/1 (ALFA)
          C=0.000008/2 (TOPMED)
          C=0.000032/1 (GnomAD)
          ...more
          HGVS:
          5.

          rs1491386466 [Homo sapiens]
            Variant type:
            DEL
            Alleles:
            TC>- [Show Flanks]
            Chromosome:
            5:8375425 (GRCh38)
            5:8375538 (GRCh37)
            Canonical SPDI:
            NC_000005.10:8375424:TC:
            Gene:
            LINC02226 (Varview)
            Functional Consequence:
            intron_variant
            Validated:
            by frequency,by alfa
            MAF:
            -=0./0 (ALFA)
            HGVS:
            6.

            rs1491369743 has merged into rs71609187 [Homo sapiens]
              Variant type:
              DELINS
              Alleles:
              TTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
              Chromosome:
              5:8454949 (GRCh38)
              5:8455062 (GRCh37)
              Canonical SPDI:
              NC_000005.10:8454938:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000005.10:8454938:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000005.10:8454938:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000005.10:8454938:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000005.10:8454938:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000005.10:8454938:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000005.10:8454938:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000005.10:8454938:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000005.10:8454938:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000005.10:8454938:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000005.10:8454938:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000005.10:8454938:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000005.10:8454938:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:8454938:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:8454938:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:8454938:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:8454938:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:8454938:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:8454938:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:8454938:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:8454938:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:8454938:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:8454938:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:8454938:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:8454938:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
              Gene:
              LINC02226 (Varview)
              Functional Consequence:
              intron_variant
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              TTTTTTTTTT=0./0 (ALFA)
              -=0.00003/8 (TOPMED)
              HGVS:
              NC_000005.10:g.8454949_8454961del, NC_000005.10:g.8454950_8454961del, NC_000005.10:g.8454951_8454961del, NC_000005.10:g.8454952_8454961del, NC_000005.10:g.8454953_8454961del, NC_000005.10:g.8454954_8454961del, NC_000005.10:g.8454955_8454961del, NC_000005.10:g.8454956_8454961del, NC_000005.10:g.8454957_8454961del, NC_000005.10:g.8454958_8454961del, NC_000005.10:g.8454959_8454961del, NC_000005.10:g.8454960_8454961del, NC_000005.10:g.8454961del, NC_000005.10:g.8454961dup, NC_000005.10:g.8454960_8454961dup, NC_000005.10:g.8454959_8454961dup, NC_000005.10:g.8454958_8454961dup, NC_000005.10:g.8454957_8454961dup, NC_000005.10:g.8454956_8454961dup, NC_000005.10:g.8454953_8454961dup, NC_000005.10:g.8454952_8454961dup, NC_000005.10:g.8454951_8454961dup, NC_000005.10:g.8454950_8454961dup, NC_000005.10:g.8454946_8454961dup, NC_000005.10:g.8454944_8454961dup, NC_000005.9:g.8455062_8455074del, NC_000005.9:g.8455063_8455074del, NC_000005.9:g.8455064_8455074del, NC_000005.9:g.8455065_8455074del, NC_000005.9:g.8455066_8455074del, NC_000005.9:g.8455067_8455074del, NC_000005.9:g.8455068_8455074del, NC_000005.9:g.8455069_8455074del, NC_000005.9:g.8455070_8455074del, NC_000005.9:g.8455071_8455074del, NC_000005.9:g.8455072_8455074del, NC_000005.9:g.8455073_8455074del, NC_000005.9:g.8455074del, NC_000005.9:g.8455074dup, NC_000005.9:g.8455073_8455074dup, NC_000005.9:g.8455072_8455074dup, NC_000005.9:g.8455071_8455074dup, NC_000005.9:g.8455070_8455074dup, NC_000005.9:g.8455069_8455074dup, NC_000005.9:g.8455066_8455074dup, NC_000005.9:g.8455065_8455074dup, NC_000005.9:g.8455064_8455074dup, NC_000005.9:g.8455063_8455074dup, NC_000005.9:g.8455059_8455074dup, NC_000005.9:g.8455057_8455074dup
              ...more
              7.

              rs1491364198 has merged into rs35855574 [Homo sapiens]
                Variant type:
                DELINS
                Alleles:
                AAAAA>-,A,AA,AAA,AAAA,AAAAAA,AAAAAAA [Show Flanks]
                Chromosome:
                5:8376421 (GRCh38)
                5:8376534 (GRCh37)
                Canonical SPDI:
                NC_000005.10:8376408:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000005.10:8376408:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000005.10:8376408:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000005.10:8376408:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000005.10:8376408:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000005.10:8376408:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000005.10:8376408:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA
                Gene:
                LINC02226 (Varview)
                Functional Consequence:
                intron_variant
                Validated:
                by frequency,by alfa,by cluster
                MAF:
                AAAAAAAAAAAAAA=0./0 (ALFA)
                AA=0.4764/2386 (1000Genomes)
                HGVS:
                8.

                rs1491362868 has merged into rs1457624732 [Homo sapiens]
                  Variant type:
                  DELINS
                  Alleles:
                  GAGA>-,GA,GAGAGA [Show Flanks]
                  Chromosome:
                  5:8363771 (GRCh38)
                  5:8363884 (GRCh37)
                  Canonical SPDI:
                  NC_000005.10:8363763:AGAGAGAGAGA:AGAGAGA,NC_000005.10:8363763:AGAGAGAGAGA:AGAGAGAGA,NC_000005.10:8363763:AGAGAGAGAGA:AGAGAGAGAGAGA
                  Gene:
                  LINC02226 (Varview)
                  Functional Consequence:
                  intron_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  AGAGAGAGA=0./0 (ALFA)
                  AG=0.000007/1 (GnomAD)
                  HGVS:
                  9.

                  rs1491295342 [Homo sapiens]
                    Variant type:
                    DELINS
                    Alleles:
                    TT>- [Show Flanks]
                    Chromosome:
                    5:8374841 (GRCh38)
                    5:8374954 (GRCh37)
                    Canonical SPDI:
                    NC_000005.10:8374837:TTTTT:TTT
                    Gene:
                    LINC02226 (Varview)
                    Functional Consequence:
                    intron_variant
                    Validated:
                    by frequency,by alfa
                    MAF:
                    TTT=0./0 (ALFA)
                    -=0.000007/1 (GnomAD)
                    HGVS:
                    10.

                    rs1491285506 [Homo sapiens]
                      Variant type:
                      DEL
                      Alleles:
                      AA>- [Show Flanks]
                      Chromosome:
                      5:8363763 (GRCh38)
                      5:8363876 (GRCh37)
                      Canonical SPDI:
                      NC_000005.10:8363762:AA:
                      Gene:
                      LINC02226 (Varview)
                      Functional Consequence:
                      intron_variant
                      Validated:
                      by frequency,by alfa,by cluster
                      MAF:
                      -=0./0 (ALFA)
                      -=0.000035/1 (TOMMO)
                      -=0.000086/12 (GnomAD)
                      ...more
                      HGVS:
                      11.

                      rs1491279016 has merged into rs200025260 [Homo sapiens]
                        Variant type:
                        DELINS
                        Alleles:
                        GGGG>-,GG,GGGGGG [Show Flanks]
                        Chromosome:
                        5:8419114 (GRCh38)
                        5:8419227 (GRCh37)
                        Canonical SPDI:
                        NC_000005.10:8419111:GGGGGG:GG,NC_000005.10:8419111:GGGGGG:GGGG,NC_000005.10:8419111:GGGGGG:GGGGGGGG
                        Gene:
                        LINC02226 (Varview)
                        Functional Consequence:
                        intron_variant
                        Validated:
                        by frequency,by alfa,by cluster
                        MAF:
                        GGGGGGGG=0./0 (ALFA)
                        GG=0.06133/1028 (TOMMO)
                        GG=0.12472/558 (Estonian)
                        GG=0.13333/80 (NorthernSweden)
                        GG=0.15/6 (GENOME_DK)
                        -=0.25454/981 (ALSPAC)
                        ...more
                        HGVS:
                        12.

                        rs1491264710 [Homo sapiens]
                          Variant type:
                          DEL
                          Alleles:
                          CA>- [Show Flanks]
                          Chromosome:
                          5:8376408 (GRCh38)
                          5:8376521 (GRCh37)
                          Canonical SPDI:
                          NC_000005.10:8376407:CA:
                          Gene:
                          LINC02226 (Varview)
                          Functional Consequence:
                          intron_variant
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          -=0.01054/125 (ALFA)
                          -=0.00071/12 (TOMMO)
                          HGVS:
                          13.

                          rs1491249249 [Homo sapiens]
                            Variant type:
                            DELINS
                            Alleles:
                            ->ATAATTTTATAATTGTATTAT [Show Flanks]
                            Chromosome:
                            5:8374838 (GRCh38)
                            5:8374952 (GRCh37)
                            Canonical SPDI:
                            NC_000005.10:8374838:TTTTATAATTGTATTAT:TTTTATAATTGTATTATATAATTTTATAATTGTATTAT
                            Gene:
                            LINC02226 (Varview)
                            Functional Consequence:
                            intron_variant
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            TTTTATAATTGTATTATATAATTTTATAATTGTATTAT=0./0 (ALFA)
                            TTTTATAATTGTATTATATAA=0.000007/1 (GnomAD)
                            TTTTATAATTGTATTATATAA=0.000011/3 (TOPMED)
                            ...more
                            HGVS:
                            14.

                            rs1491248026 has merged into rs1301042503 [Homo sapiens]
                              Variant type:
                              DELINS
                              Alleles:
                              GTTT>-,GTTTAATTTGTTT [Show Flanks]
                              Chromosome:
                              5:8353892 (GRCh38)
                              5:8354005 (GRCh37)
                              Canonical SPDI:
                              NC_000005.10:8353888:TTTGTTT:TTT,NC_000005.10:8353888:TTTGTTT:TTTGTTTAATTTGTTT
                              Gene:
                              LINC02226 (Varview)
                              Functional Consequence:
                              intron_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              TTTGTTTAATTTGTTT=0./0 (ALFA)
                              HGVS:
                              15.

                              rs1491148921 has merged into rs200025260 [Homo sapiens]
                                Variant type:
                                DELINS
                                Alleles:
                                GGGG>-,GG,GGGGGG [Show Flanks]
                                Chromosome:
                                5:8419114 (GRCh38)
                                5:8419227 (GRCh37)
                                Canonical SPDI:
                                NC_000005.10:8419111:GGGGGG:GG,NC_000005.10:8419111:GGGGGG:GGGG,NC_000005.10:8419111:GGGGGG:GGGGGGGG
                                Gene:
                                LINC02226 (Varview)
                                Functional Consequence:
                                intron_variant
                                Validated:
                                by frequency,by alfa,by cluster
                                MAF:
                                GGGGGGGG=0./0 (ALFA)
                                GG=0.06133/1028 (TOMMO)
                                GG=0.12472/558 (Estonian)
                                GG=0.13333/80 (NorthernSweden)
                                GG=0.15/6 (GENOME_DK)
                                -=0.25454/981 (ALSPAC)
                                ...more
                                HGVS:
                                16.

                                rs1491095258 [Homo sapiens]
                                  Variant type:
                                  SNV:
                                  Alleles:
                                  GG>-
                                  Chromosome:
                                  no mapping
                                  Canonical SPDI:
                                  17.

                                  rs1491054905 has merged into rs34800047 [Homo sapiens]
                                    Variant type:
                                    DELINS
                                    Alleles:
                                    TT>-,T,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTTT,TTTTTTTTTTTTT [Show Flanks]
                                    Chromosome:
                                    5:8400521 (GRCh38)
                                    5:8400634 (GRCh37)
                                    Canonical SPDI:
                                    NC_000005.10:8400509:TTTTTTTTTTTTT:TTTTTTTTTTT,NC_000005.10:8400509:TTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000005.10:8400509:TTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000005.10:8400509:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000005.10:8400509:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000005.10:8400509:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000005.10:8400509:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000005.10:8400509:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000005.10:8400509:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT
                                    Gene:
                                    LINC02226 (Varview)
                                    Functional Consequence:
                                    intron_variant
                                    Validated:
                                    by frequency,by alfa,by cluster
                                    MAF:
                                    TTTTTTTTTTTTTTTTT=0./0 (ALFA)
                                    HGVS:
                                    18.

                                    rs1491042725 has merged into rs35736363 [Homo sapiens]
                                      Variant type:
                                      DELINS
                                      Alleles:
                                      ATATAT>-,AT,ATAT,ATATATAT,ATATATATAT,ATATATATATAT,ATATATATATATAT,ATATATATATATATAT,ATATATATATATATATAT,ATATATATATATATATATAT,ATATATATATATATATATATATAT,ATATATATATATATATATATATATAT [Show Flanks]
                                      Chromosome:
                                      5:8375420 (GRCh38)
                                      5:8375533 (GRCh37)
                                      Canonical SPDI:
                                      NC_000005.10:8375404:TATATATATATATATATATAT:TATATATATATATAT,NC_000005.10:8375404:TATATATATATATATATATAT:TATATATATATATATAT,NC_000005.10:8375404:TATATATATATATATATATAT:TATATATATATATATATAT,NC_000005.10:8375404:TATATATATATATATATATAT:TATATATATATATATATATATAT,NC_000005.10:8375404:TATATATATATATATATATAT:TATATATATATATATATATATATAT,NC_000005.10:8375404:TATATATATATATATATATAT:TATATATATATATATATATATATATAT,NC_000005.10:8375404:TATATATATATATATATATAT:TATATATATATATATATATATATATATAT,NC_000005.10:8375404:TATATATATATATATATATAT:TATATATATATATATATATATATATATATAT,NC_000005.10:8375404:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATAT,NC_000005.10:8375404:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATATAT,NC_000005.10:8375404:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATATATATAT,NC_000005.10:8375404:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATATATATATAT
                                      Gene:
                                      LINC02226 (Varview)
                                      Functional Consequence:
                                      intron_variant
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      TATATATATATATATAT=0./0 (ALFA)
                                      TATATATATATATATATA=0.000004/1 (TOPMED)
                                      HGVS:
                                      19.

                                      rs1490992391 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        A>G,T [Show Flanks]
                                        Chromosome:
                                        5:8425816 (GRCh38)
                                        5:8425929 (GRCh37)
                                        Canonical SPDI:
                                        NC_000005.10:8425815:A:G,NC_000005.10:8425815:A:T
                                        Gene:
                                        LINC02226 (Varview)
                                        Functional Consequence:
                                        intron_variant
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        T=0./0 (ALFA)
                                        G=0.000029/4 (GnomAD)
                                        HGVS:
                                        20.

                                        rs1490977582 [Homo sapiens]
                                          Variant type:
                                          DELINS
                                          Alleles:
                                          ->T [Show Flanks]
                                          Chromosome:
                                          5:8427905 (GRCh38)
                                          5:8428019 (GRCh37)
                                          Canonical SPDI:
                                          NC_000005.10:8427905:T:TT
                                          Gene:
                                          LINC02226 (Varview)
                                          Functional Consequence:
                                          intron_variant
                                          Validated:
                                          by frequency,by alfa,by cluster
                                          MAF:
                                          TT=0./0 (ALFA)
                                          T=0.000014/2 (GnomAD)
                                          T=0.000019/5 (TOPMED)
                                          ...more
                                          HGVS:

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