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Items: 1 to 20 of 571

1.

rs1490543688 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    C>T [Show Flanks]
    Chromosome:
    11:122091032 (GRCh38)
    11:121961740 (GRCh37)
    Canonical SPDI:
    NC_000011.10:122091031:C:T
    Gene:
    MIR100HG (Varview)
    Functional Consequence:
    non_coding_transcript_variant,intron_variant
    Validated:
    by frequency,by alfa
    MAF:
    T=0./0 (ALFA)
    T=0.000007/1 (GnomAD)
    HGVS:

    2.

    rs1490484468 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      C>T [Show Flanks]
      Chromosome:
      11:122091419 (GRCh38)
      11:121962127 (GRCh37)
      Canonical SPDI:
      NC_000011.10:122091418:C:T
      Gene:
      MIR100HG (Varview)
      Functional Consequence:
      non_coding_transcript_variant,intron_variant
      Validated:
      by frequency,by alfa
      MAF:
      T=0./0 (ALFA)
      T=0.000008/2 (TOPMED)
      HGVS:

      3.

      rs1490406624 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        G>A,T [Show Flanks]
        Chromosome:
        11:122090219 (GRCh38)
        11:121960927 (GRCh37)
        Canonical SPDI:
        NC_000011.10:122090218:G:A,NC_000011.10:122090218:G:T
        Gene:
        MIR100HG (Varview)
        Functional Consequence:
        non_coding_transcript_variant,intron_variant
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        A=0./0 (ALFA)
        A=0.00006/2 (GnomAD)
        A=0.01745/51 (KOREAN)
        HGVS:
        NC_000011.10:g.122090219G>A, NC_000011.10:g.122090219G>T, NC_000011.9:g.121960927G>A, NC_000011.9:g.121960927G>T, NR_024430.2:n.2013C>T, NR_024430.2:n.2013C>A, NR_024430.1:n.1966C>T, NR_024430.1:n.1966C>A, NR_137190.1:n.2338C>T, NR_137190.1:n.2338C>A, NR_137191.1:n.2317C>T, NR_137191.1:n.2317C>A, NR_137189.1:n.2305C>T, NR_137189.1:n.2305C>A, NR_137175.1:n.2284C>T, NR_137175.1:n.2284C>A, NR_137192.1:n.2177C>T, NR_137192.1:n.2177C>A, NR_137196.1:n.2068C>T, NR_137196.1:n.2068C>A, NR_137195.1:n.2047C>T, NR_137195.1:n.2047C>A, NR_137180.1:n.2025C>T, NR_137180.1:n.2025C>A, NR_137193.1:n.2004C>T, NR_137193.1:n.2004C>A, NR_137176.1:n.1995C>T, NR_137176.1:n.1995C>A, NR_137182.1:n.1992C>T, NR_137182.1:n.1992C>A, NR_137177.1:n.1974C>T, NR_137177.1:n.1974C>A, NR_137179.1:n.1967C>T, NR_137179.1:n.1967C>A, NR_137181.1:n.1910C>T, NR_137181.1:n.1910C>A, NR_137183.1:n.1901C>T, NR_137183.1:n.1901C>A, NR_137185.1:n.1880C>T, NR_137185.1:n.1880C>A, NR_137194.1:n.1879C>T, NR_137194.1:n.1879C>A, NR_137188.1:n.1858C>T, NR_137188.1:n.1858C>A, NR_137184.1:n.1819C>T, NR_137184.1:n.1819C>A, NR_137186.1:n.1789C>T, NR_137186.1:n.1789C>A, NR_137187.1:n.1768C>T, NR_137187.1:n.1768C>A

        4.

        rs1489977830 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          G>A,T [Show Flanks]
          Chromosome:
          11:122090922 (GRCh38)
          11:121961630 (GRCh37)
          Canonical SPDI:
          NC_000011.10:122090921:G:A,NC_000011.10:122090921:G:T
          Gene:
          MIR100HG (Varview)
          Functional Consequence:
          non_coding_transcript_variant,intron_variant
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          T=0./0 (ALFA)
          A=0.000004/1 (TOPMED)
          HGVS:
          NC_000011.10:g.122090922G>A, NC_000011.10:g.122090922G>T, NC_000011.9:g.121961630G>A, NC_000011.9:g.121961630G>T, NR_024430.2:n.1310C>T, NR_024430.2:n.1310C>A, NR_024430.1:n.1263C>T, NR_024430.1:n.1263C>A, NR_137190.1:n.1635C>T, NR_137190.1:n.1635C>A, NR_137191.1:n.1614C>T, NR_137191.1:n.1614C>A, NR_137189.1:n.1602C>T, NR_137189.1:n.1602C>A, NR_137175.1:n.1581C>T, NR_137175.1:n.1581C>A, NR_137192.1:n.1474C>T, NR_137192.1:n.1474C>A, NR_137196.1:n.1365C>T, NR_137196.1:n.1365C>A, NR_137195.1:n.1344C>T, NR_137195.1:n.1344C>A, NR_137180.1:n.1322C>T, NR_137180.1:n.1322C>A, NR_137193.1:n.1301C>T, NR_137193.1:n.1301C>A, NR_137176.1:n.1292C>T, NR_137176.1:n.1292C>A, NR_137182.1:n.1289C>T, NR_137182.1:n.1289C>A, NR_137177.1:n.1271C>T, NR_137177.1:n.1271C>A, NR_137179.1:n.1264C>T, NR_137179.1:n.1264C>A, NR_137181.1:n.1207C>T, NR_137181.1:n.1207C>A, NR_137183.1:n.1198C>T, NR_137183.1:n.1198C>A, NR_137185.1:n.1177C>T, NR_137185.1:n.1177C>A, NR_137194.1:n.1176C>T, NR_137194.1:n.1176C>A, NR_137188.1:n.1155C>T, NR_137188.1:n.1155C>A, NR_137184.1:n.1116C>T, NR_137184.1:n.1116C>A, NR_137186.1:n.1086C>T, NR_137186.1:n.1086C>A, NR_137187.1:n.1065C>T, NR_137187.1:n.1065C>A

          5.

          rs1489823867 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            C>T [Show Flanks]
            Chromosome:
            11:122089461 (GRCh38)
            11:121960169 (GRCh37)
            Canonical SPDI:
            NC_000011.10:122089460:C:T
            Gene:
            MIR100HG (Varview)
            Functional Consequence:
            non_coding_transcript_variant,intron_variant
            Validated:
            by frequency,by alfa,by cluster
            MAF:
            T=0./0 (ALFA)
            T=0.000014/2 (GnomAD)
            T=0.000026/7 (TOPMED)
            HGVS:

            6.

            rs1488526865 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              T>C [Show Flanks]
              Chromosome:
              11:122180554 (GRCh38)
              11:122051262 (GRCh37)
              Canonical SPDI:
              NC_000011.10:122180553:T:C
              Gene:
              MIR100HG (Varview)
              Functional Consequence:
              non_coding_transcript_variant,genic_upstream_transcript_variant,intron_variant
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              C=0./0 (ALFA)
              C=0.000008/2 (TOPMED)
              HGVS:

              7.

              rs1488027031 [Homo sapiens]
                Variant type:
                DELINS
                Alleles:
                ->AA [Show Flanks]
                Chromosome:
                11:122090246 (GRCh38)
                11:121960955 (GRCh37)
                Canonical SPDI:
                NC_000011.10:122090246:AAA:AAAAA
                Gene:
                MIR100HG (Varview)
                Functional Consequence:
                non_coding_transcript_variant,intron_variant
                Validated:
                by frequency,by cluster
                MAF:
                AA=0.00072/12 (TOMMO)
                HGVS:

                8.

                rs1485077726 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  A>G,T [Show Flanks]
                  Chromosome:
                  11:122090366 (GRCh38)
                  11:121961074 (GRCh37)
                  Canonical SPDI:
                  NC_000011.10:122090365:A:G,NC_000011.10:122090365:A:T
                  Gene:
                  MIR100HG (Varview)
                  Functional Consequence:
                  non_coding_transcript_variant,intron_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  T=0.00022/1 (ALFA)
                  G=0.00004/1 (TOMMO)
                  T=0.00022/1 (Estonian)
                  HGVS:
                  NC_000011.10:g.122090366A>G, NC_000011.10:g.122090366A>T, NC_000011.9:g.121961074A>G, NC_000011.9:g.121961074A>T, NR_024430.2:n.1866T>C, NR_024430.2:n.1866T>A, NR_024430.1:n.1819T>C, NR_024430.1:n.1819T>A, NR_137190.1:n.2191T>C, NR_137190.1:n.2191T>A, NR_137191.1:n.2170T>C, NR_137191.1:n.2170T>A, NR_137189.1:n.2158T>C, NR_137189.1:n.2158T>A, NR_137175.1:n.2137T>C, NR_137175.1:n.2137T>A, NR_137192.1:n.2030T>C, NR_137192.1:n.2030T>A, NR_137196.1:n.1921T>C, NR_137196.1:n.1921T>A, NR_137195.1:n.1900T>C, NR_137195.1:n.1900T>A, NR_137180.1:n.1878T>C, NR_137180.1:n.1878T>A, NR_137193.1:n.1857T>C, NR_137193.1:n.1857T>A, NR_137176.1:n.1848T>C, NR_137176.1:n.1848T>A, NR_137182.1:n.1845T>C, NR_137182.1:n.1845T>A, NR_137177.1:n.1827T>C, NR_137177.1:n.1827T>A, NR_137179.1:n.1820T>C, NR_137179.1:n.1820T>A, NR_137181.1:n.1763T>C, NR_137181.1:n.1763T>A, NR_137183.1:n.1754T>C, NR_137183.1:n.1754T>A, NR_137185.1:n.1733T>C, NR_137185.1:n.1733T>A, NR_137194.1:n.1732T>C, NR_137194.1:n.1732T>A, NR_137188.1:n.1711T>C, NR_137188.1:n.1711T>A, NR_137184.1:n.1672T>C, NR_137184.1:n.1672T>A, NR_137186.1:n.1642T>C, NR_137186.1:n.1642T>A, NR_137187.1:n.1621T>C, NR_137187.1:n.1621T>A

                  9.

                  rs1483945742 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    T>C [Show Flanks]
                    Chromosome:
                    11:122090323 (GRCh38)
                    11:121961031 (GRCh37)
                    Canonical SPDI:
                    NC_000011.10:122090322:T:C
                    Gene:
                    MIR100HG (Varview)
                    Functional Consequence:
                    intron_variant,non_coding_transcript_variant
                    Validated:
                    by frequency,by alfa,by cluster
                    MAF:
                    C=0./0 (ALFA)
                    C=0.000004/1 (TOPMED)
                    C=0.000007/1 (GnomAD)
                    HGVS:

                    10.

                    rs1481976954 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      T>C [Show Flanks]
                      Chromosome:
                      11:122089424 (GRCh38)
                      11:121960132 (GRCh37)
                      Canonical SPDI:
                      NC_000011.10:122089423:T:C
                      Gene:
                      MIR100HG (Varview)
                      Functional Consequence:
                      intron_variant,non_coding_transcript_variant
                      Validated:
                      by frequency,by alfa,by cluster
                      MAF:
                      C=0./0 (ALFA)
                      C=0.000011/3 (TOPMED)
                      C=0.000014/2 (GnomAD)
                      HGVS:

                      11.

                      rs1481296322 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        G>A [Show Flanks]
                        Chromosome:
                        11:122091548 (GRCh38)
                        11:121962256 (GRCh37)
                        Canonical SPDI:
                        NC_000011.10:122091547:G:A
                        Gene:
                        MIR100HG (Varview)
                        Functional Consequence:
                        intron_variant,non_coding_transcript_variant
                        Validated:
                        by frequency,by alfa
                        MAF:
                        A=0./0 (ALFA)
                        A=0.000004/1 (TOPMED)
                        HGVS:

                        12.

                        rs1480792324 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          T>A,C [Show Flanks]
                          Chromosome:
                          11:122090723 (GRCh38)
                          11:121961431 (GRCh37)
                          Canonical SPDI:
                          NC_000011.10:122090722:T:A,NC_000011.10:122090722:T:C
                          Gene:
                          MIR100HG (Varview)
                          Functional Consequence:
                          intron_variant,non_coding_transcript_variant
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          A=0.000071/1 (ALFA)
                          A=0.000008/2 (TOPMED)
                          HGVS:
                          NC_000011.10:g.122090723T>A, NC_000011.10:g.122090723T>C, NC_000011.9:g.121961431T>A, NC_000011.9:g.121961431T>C, NR_024430.2:n.1509A>T, NR_024430.2:n.1509A>G, NR_024430.1:n.1462A>T, NR_024430.1:n.1462A>G, NR_137190.1:n.1834A>T, NR_137190.1:n.1834A>G, NR_137191.1:n.1813A>T, NR_137191.1:n.1813A>G, NR_137189.1:n.1801A>T, NR_137189.1:n.1801A>G, NR_137175.1:n.1780A>T, NR_137175.1:n.1780A>G, NR_137192.1:n.1673A>T, NR_137192.1:n.1673A>G, NR_137196.1:n.1564A>T, NR_137196.1:n.1564A>G, NR_137195.1:n.1543A>T, NR_137195.1:n.1543A>G, NR_137180.1:n.1521A>T, NR_137180.1:n.1521A>G, NR_137193.1:n.1500A>T, NR_137193.1:n.1500A>G, NR_137176.1:n.1491A>T, NR_137176.1:n.1491A>G, NR_137182.1:n.1488A>T, NR_137182.1:n.1488A>G, NR_137177.1:n.1470A>T, NR_137177.1:n.1470A>G, NR_137179.1:n.1463A>T, NR_137179.1:n.1463A>G, NR_137181.1:n.1406A>T, NR_137181.1:n.1406A>G, NR_137183.1:n.1397A>T, NR_137183.1:n.1397A>G, NR_137185.1:n.1376A>T, NR_137185.1:n.1376A>G, NR_137194.1:n.1375A>T, NR_137194.1:n.1375A>G, NR_137188.1:n.1354A>T, NR_137188.1:n.1354A>G, NR_137184.1:n.1315A>T, NR_137184.1:n.1315A>G, NR_137186.1:n.1285A>T, NR_137186.1:n.1285A>G, NR_137187.1:n.1264A>T, NR_137187.1:n.1264A>G

                          13.

                          rs1479410111 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            T>C [Show Flanks]
                            Chromosome:
                            11:122091721 (GRCh38)
                            11:121962429 (GRCh37)
                            Canonical SPDI:
                            NC_000011.10:122091720:T:C
                            Gene:
                            MIR100HG (Varview)
                            Functional Consequence:
                            intron_variant,splice_acceptor_variant,non_coding_transcript_variant
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            C=0./0 (ALFA)
                            C=0.000007/1 (GnomAD)
                            C=0.000011/3 (TOPMED)
                            HGVS:

                            14.

                            rs1479266888 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              T>C [Show Flanks]
                              Chromosome:
                              11:122089924 (GRCh38)
                              11:121960632 (GRCh37)
                              Canonical SPDI:
                              NC_000011.10:122089923:T:C
                              Gene:
                              MIR100HG (Varview)
                              Functional Consequence:
                              intron_variant,non_coding_transcript_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              C=0./0 (ALFA)
                              C=0.000014/2 (GnomAD)
                              C=0.00003/8 (TOPMED)
                              HGVS:

                              15.

                              rs1478823862 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                C>A,T [Show Flanks]
                                Chromosome:
                                11:122090908 (GRCh38)
                                11:121961616 (GRCh37)
                                Canonical SPDI:
                                NC_000011.10:122090907:C:A,NC_000011.10:122090907:C:T
                                Gene:
                                MIR100HG (Varview)
                                Functional Consequence:
                                intron_variant,non_coding_transcript_variant
                                Validated:
                                by frequency,by alfa,by cluster
                                MAF:
                                A=0./0 (ALFA)
                                A=0.000007/1 (GnomAD)
                                A=0.000008/2 (TOPMED)
                                HGVS:
                                NC_000011.10:g.122090908C>A, NC_000011.10:g.122090908C>T, NC_000011.9:g.121961616C>A, NC_000011.9:g.121961616C>T, NR_024430.2:n.1324G>T, NR_024430.2:n.1324G>A, NR_024430.1:n.1277G>T, NR_024430.1:n.1277G>A, NR_137190.1:n.1649G>T, NR_137190.1:n.1649G>A, NR_137191.1:n.1628G>T, NR_137191.1:n.1628G>A, NR_137189.1:n.1616G>T, NR_137189.1:n.1616G>A, NR_137175.1:n.1595G>T, NR_137175.1:n.1595G>A, NR_137192.1:n.1488G>T, NR_137192.1:n.1488G>A, NR_137196.1:n.1379G>T, NR_137196.1:n.1379G>A, NR_137195.1:n.1358G>T, NR_137195.1:n.1358G>A, NR_137180.1:n.1336G>T, NR_137180.1:n.1336G>A, NR_137193.1:n.1315G>T, NR_137193.1:n.1315G>A, NR_137176.1:n.1306G>T, NR_137176.1:n.1306G>A, NR_137182.1:n.1303G>T, NR_137182.1:n.1303G>A, NR_137177.1:n.1285G>T, NR_137177.1:n.1285G>A, NR_137179.1:n.1278G>T, NR_137179.1:n.1278G>A, NR_137181.1:n.1221G>T, NR_137181.1:n.1221G>A, NR_137183.1:n.1212G>T, NR_137183.1:n.1212G>A, NR_137185.1:n.1191G>T, NR_137185.1:n.1191G>A, NR_137194.1:n.1190G>T, NR_137194.1:n.1190G>A, NR_137188.1:n.1169G>T, NR_137188.1:n.1169G>A, NR_137184.1:n.1130G>T, NR_137184.1:n.1130G>A, NR_137186.1:n.1100G>T, NR_137186.1:n.1100G>A, NR_137187.1:n.1079G>T, NR_137187.1:n.1079G>A

                                16.

                                rs1476776282 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  T>G [Show Flanks]
                                  Chromosome:
                                  11:122089260 (GRCh38)
                                  11:121959968 (GRCh37)
                                  Canonical SPDI:
                                  NC_000011.10:122089259:T:G
                                  Gene:
                                  MIR100HG (Varview)
                                  Functional Consequence:
                                  intron_variant,non_coding_transcript_variant
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  G=0./0 (ALFA)
                                  G=0.000014/2 (GnomAD)
                                  G=0.000015/4 (TOPMED)
                                  G=0.000684/2 (KOREAN)
                                  HGVS:

                                  17.

                                  rs1475485100 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    T>C [Show Flanks]
                                    Chromosome:
                                    11:122090786 (GRCh38)
                                    11:121961494 (GRCh37)
                                    Canonical SPDI:
                                    NC_000011.10:122090785:T:C
                                    Gene:
                                    MIR100HG (Varview)
                                    Functional Consequence:
                                    intron_variant,non_coding_transcript_variant
                                    Validated:
                                    by frequency,by alfa
                                    MAF:
                                    C=0./0 (ALFA)
                                    HGVS:

                                    18.

                                    rs1473429796 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      A>G [Show Flanks]
                                      Chromosome:
                                      11:122090092 (GRCh38)
                                      11:121960800 (GRCh37)
                                      Canonical SPDI:
                                      NC_000011.10:122090091:A:G
                                      Gene:
                                      MIR100HG (Varview)
                                      Functional Consequence:
                                      intron_variant,non_coding_transcript_variant
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      G=0./0 (ALFA)
                                      G=0.000004/1 (TOPMED)
                                      G=0.000007/1 (GnomAD)
                                      HGVS:

                                      19.

                                      rs1470782869 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        G>A,T [Show Flanks]
                                        Chromosome:
                                        11:122089293 (GRCh38)
                                        11:121960001 (GRCh37)
                                        Canonical SPDI:
                                        NC_000011.10:122089292:G:A,NC_000011.10:122089292:G:T
                                        Gene:
                                        MIR100HG (Varview)
                                        Functional Consequence:
                                        intron_variant,non_coding_transcript_variant
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        T=0./0 (ALFA)
                                        T=0.000023/6 (TOPMED)
                                        A=0.000035/1 (TOMMO)
                                        HGVS:
                                        NC_000011.10:g.122089293G>A, NC_000011.10:g.122089293G>T, NC_000011.9:g.121960001G>A, NC_000011.9:g.121960001G>T, NR_024430.2:n.2939C>T, NR_024430.2:n.2939C>A, NR_024430.1:n.2892C>T, NR_024430.1:n.2892C>A, NR_137190.1:n.3264C>T, NR_137190.1:n.3264C>A, NR_137191.1:n.3243C>T, NR_137191.1:n.3243C>A, NR_137189.1:n.3231C>T, NR_137189.1:n.3231C>A, NR_137175.1:n.3210C>T, NR_137175.1:n.3210C>A, NR_137192.1:n.3103C>T, NR_137192.1:n.3103C>A, NR_137196.1:n.2994C>T, NR_137196.1:n.2994C>A, NR_137195.1:n.2973C>T, NR_137195.1:n.2973C>A, NR_137180.1:n.2951C>T, NR_137180.1:n.2951C>A, NR_137193.1:n.2930C>T, NR_137193.1:n.2930C>A, NR_137176.1:n.2921C>T, NR_137176.1:n.2921C>A, NR_137182.1:n.2918C>T, NR_137182.1:n.2918C>A, NR_137177.1:n.2900C>T, NR_137177.1:n.2900C>A, NR_137179.1:n.2893C>T, NR_137179.1:n.2893C>A, NR_137181.1:n.2836C>T, NR_137181.1:n.2836C>A, NR_137183.1:n.2827C>T, NR_137183.1:n.2827C>A, NR_137185.1:n.2806C>T, NR_137185.1:n.2806C>A, NR_137194.1:n.2805C>T, NR_137194.1:n.2805C>A, NR_137188.1:n.2784C>T, NR_137188.1:n.2784C>A, NR_137184.1:n.2745C>T, NR_137184.1:n.2745C>A, NR_137186.1:n.2715C>T, NR_137186.1:n.2715C>A, NR_137187.1:n.2694C>T, NR_137187.1:n.2694C>A

                                        20.

                                        rs1470458942 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          C>G [Show Flanks]
                                          Chromosome:
                                          11:122090454 (GRCh38)
                                          11:121961162 (GRCh37)
                                          Canonical SPDI:
                                          NC_000011.10:122090453:C:G
                                          Gene:
                                          MIR100HG (Varview)
                                          Functional Consequence:
                                          intron_variant,non_coding_transcript_variant
                                          Validated:
                                          by frequency,by alfa
                                          MAF:
                                          G=0./0 (ALFA)
                                          G=0.000007/1 (GnomAD)
                                          HGVS:

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