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Items: 1 to 20 of 8305

1.

rs1491119411 has merged into rs11340393 [Homo sapiens]
    Variant type:
    DELINS
    Alleles:
    TTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
    Chromosome:
    4:69200324 (GRCh38)
    4:70066042 (GRCh37)
    Canonical SPDI:
    NC_000004.12:69200312:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000004.12:69200312:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000004.12:69200312:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000004.12:69200312:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000004.12:69200312:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000004.12:69200312:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000004.12:69200312:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000004.12:69200312:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000004.12:69200312:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000004.12:69200312:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000004.12:69200312:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000004.12:69200312:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:69200312:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:69200312:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:69200312:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:69200312:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:69200312:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:69200312:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:69200312:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:69200312:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:69200312:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:69200312:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:69200312:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:69200312:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:69200312:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
    Gene:
    UGT2B11 (Varview), LOC105377267 (Varview)
    Functional Consequence:
    intron_variant,3_prime_UTR_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    TTTTTTTTTTTTT=0./0 (ALFA)
    HGVS:
    NC_000004.12:g.69200324_69200334del, NC_000004.12:g.69200325_69200334del, NC_000004.12:g.69200326_69200334del, NC_000004.12:g.69200327_69200334del, NC_000004.12:g.69200328_69200334del, NC_000004.12:g.69200329_69200334del, NC_000004.12:g.69200330_69200334del, NC_000004.12:g.69200331_69200334del, NC_000004.12:g.69200332_69200334del, NC_000004.12:g.69200333_69200334del, NC_000004.12:g.69200334del, NC_000004.12:g.69200334dup, NC_000004.12:g.69200333_69200334dup, NC_000004.12:g.69200332_69200334dup, NC_000004.12:g.69200331_69200334dup, NC_000004.12:g.69200330_69200334dup, NC_000004.12:g.69200329_69200334dup, NC_000004.12:g.69200328_69200334dup, NC_000004.12:g.69200327_69200334dup, NC_000004.12:g.69200326_69200334dup, NC_000004.12:g.69200325_69200334dup, NC_000004.12:g.69200324_69200334dup, NC_000004.12:g.69200322_69200334dup, NC_000004.12:g.69200321_69200334dup, NC_000004.12:g.69200334_69200335insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.70066042_70066052del, NC_000004.11:g.70066043_70066052del, NC_000004.11:g.70066044_70066052del, NC_000004.11:g.70066045_70066052del, NC_000004.11:g.70066046_70066052del, NC_000004.11:g.70066047_70066052del, NC_000004.11:g.70066048_70066052del, NC_000004.11:g.70066049_70066052del, NC_000004.11:g.70066050_70066052del, NC_000004.11:g.70066051_70066052del, NC_000004.11:g.70066052del, NC_000004.11:g.70066052dup, NC_000004.11:g.70066051_70066052dup, NC_000004.11:g.70066050_70066052dup, NC_000004.11:g.70066049_70066052dup, NC_000004.11:g.70066048_70066052dup, NC_000004.11:g.70066047_70066052dup, NC_000004.11:g.70066046_70066052dup, NC_000004.11:g.70066045_70066052dup, NC_000004.11:g.70066044_70066052dup, NC_000004.11:g.70066043_70066052dup, NC_000004.11:g.70066042_70066052dup, NC_000004.11:g.70066040_70066052dup, NC_000004.11:g.70066039_70066052dup, NC_000004.11:g.70066052_70066053insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001073.3:c.*117_*127del, NM_001073.3:c.*118_*127del, NM_001073.3:c.*119_*127del, NM_001073.3:c.*120_*127del, NM_001073.3:c.*121_*127del, NM_001073.3:c.*122_*127del, NM_001073.3:c.*123_*127del, NM_001073.3:c.*124_*127del, NM_001073.3:c.*125_*127del, NM_001073.3:c.*126_*127del, NM_001073.3:c.*127del, NM_001073.3:c.*127dup, NM_001073.3:c.*126_*127dup, NM_001073.3:c.*125_*127dup, NM_001073.3:c.*124_*127dup, NM_001073.3:c.*123_*127dup, NM_001073.3:c.*122_*127dup, NM_001073.3:c.*121_*127dup, NM_001073.3:c.*120_*127dup, NM_001073.3:c.*119_*127dup, NM_001073.3:c.*118_*127dup, NM_001073.3:c.*117_*127dup, NM_001073.3:c.*115_*127dup, NM_001073.3:c.*114_*127dup, NM_001073.3:c.*127_*128insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_001073.2:c.*117_*127del, NM_001073.2:c.*118_*127del, NM_001073.2:c.*119_*127del, NM_001073.2:c.*120_*127del, NM_001073.2:c.*121_*127del, NM_001073.2:c.*122_*127del, NM_001073.2:c.*123_*127del, NM_001073.2:c.*124_*127del, NM_001073.2:c.*125_*127del, NM_001073.2:c.*126_*127del, NM_001073.2:c.*127del, NM_001073.2:c.*127dup, NM_001073.2:c.*126_*127dup, NM_001073.2:c.*125_*127dup, NM_001073.2:c.*124_*127dup, NM_001073.2:c.*123_*127dup, NM_001073.2:c.*122_*127dup, NM_001073.2:c.*121_*127dup, NM_001073.2:c.*120_*127dup, NM_001073.2:c.*119_*127dup, NM_001073.2:c.*118_*127dup, NM_001073.2:c.*117_*127dup, NM_001073.2:c.*115_*127dup, NM_001073.2:c.*114_*127dup, NM_001073.2:c.*127_*128insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_001073.1:c.*120_*123dup, NM_001073.1:c.*117_*123del, NM_001073.1:c.*118_*123del, NM_001073.1:c.*119_*123del, NM_001073.1:c.*120_*123del, NM_001073.1:c.*121_*123del, NM_001073.1:c.*122_*123del, NM_001073.1:c.*123del, NM_001073.1:c.*123dup, NM_001073.1:c.*122_*123dup, NM_001073.1:c.*121_*123dup, NM_001073.1:c.*119_*123dup, NM_001073.1:c.*118_*123dup, NM_001073.1:c.*117_*123dup, NM_001073.1:c.*116_*123dup, NM_001073.1:c.*115_*123dup, NM_001073.1:c.*114_*123dup, NM_001073.1:c.*113_*123dup, NM_001073.1:c.*112_*123dup, NM_001073.1:c.*111_*123dup, NM_001073.1:c.*110_*123dup, NM_001073.1:c.*109_*123dup, NM_001073.1:c.*107_*123dup, NM_001073.1:c.*106_*123dup, NM_001073.1:c.*123_*124insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XM_011531550.3:c.*117_*127del, XM_011531550.3:c.*118_*127del, XM_011531550.3:c.*119_*127del, XM_011531550.3:c.*120_*127del, XM_011531550.3:c.*121_*127del, XM_011531550.3:c.*122_*127del, XM_011531550.3:c.*123_*127del, XM_011531550.3:c.*124_*127del, XM_011531550.3:c.*125_*127del, XM_011531550.3:c.*126_*127del, XM_011531550.3:c.*127del, XM_011531550.3:c.*127dup, XM_011531550.3:c.*126_*127dup, XM_011531550.3:c.*125_*127dup, XM_011531550.3:c.*124_*127dup, XM_011531550.3:c.*123_*127dup, XM_011531550.3:c.*122_*127dup, XM_011531550.3:c.*121_*127dup, XM_011531550.3:c.*120_*127dup, XM_011531550.3:c.*119_*127dup, XM_011531550.3:c.*118_*127dup, XM_011531550.3:c.*117_*127dup, XM_011531550.3:c.*115_*127dup, XM_011531550.3:c.*114_*127dup, XM_011531550.3:c.*127_*128insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XM_011531550.1:c.*117_*127del, XM_011531550.1:c.*118_*127del, XM_011531550.1:c.*119_*127del, XM_011531550.1:c.*120_*127del, XM_011531550.1:c.*121_*127del, XM_011531550.1:c.*122_*127del, XM_011531550.1:c.*123_*127del, XM_011531550.1:c.*124_*127del, XM_011531550.1:c.*125_*127del, XM_011531550.1:c.*126_*127del, XM_011531550.1:c.*127del, XM_011531550.1:c.*127dup, XM_011531550.1:c.*126_*127dup, XM_011531550.1:c.*125_*127dup, XM_011531550.1:c.*124_*127dup, XM_011531550.1:c.*123_*127dup, XM_011531550.1:c.*122_*127dup, XM_011531550.1:c.*121_*127dup, XM_011531550.1:c.*120_*127dup, XM_011531550.1:c.*119_*127dup, XM_011531550.1:c.*118_*127dup, XM_011531550.1:c.*117_*127dup, XM_011531550.1:c.*115_*127dup, XM_011531550.1:c.*114_*127dup, XM_011531550.1:c.*127_*128insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XM_017007660.3:c.*117_*127del, XM_017007660.3:c.*118_*127del, XM_017007660.3:c.*119_*127del, XM_017007660.3:c.*120_*127del, XM_017007660.3:c.*121_*127del, XM_017007660.3:c.*122_*127del, XM_017007660.3:c.*123_*127del, XM_017007660.3:c.*124_*127del, XM_017007660.3:c.*125_*127del, XM_017007660.3:c.*126_*127del, XM_017007660.3:c.*127del, XM_017007660.3:c.*127dup, XM_017007660.3:c.*126_*127dup, XM_017007660.3:c.*125_*127dup, XM_017007660.3:c.*124_*127dup, XM_017007660.3:c.*123_*127dup, XM_017007660.3:c.*122_*127dup, XM_017007660.3:c.*121_*127dup, XM_017007660.3:c.*120_*127dup, XM_017007660.3:c.*119_*127dup, XM_017007660.3:c.*118_*127dup, XM_017007660.3:c.*117_*127dup, XM_017007660.3:c.*115_*127dup, XM_017007660.3:c.*114_*127dup, XM_017007660.3:c.*127_*128insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XM_047449543.1:c.*117_*127del, XM_047449543.1:c.*118_*127del, XM_047449543.1:c.*119_*127del, XM_047449543.1:c.*120_*127del, XM_047449543.1:c.*121_*127del, XM_047449543.1:c.*122_*127del, XM_047449543.1:c.*123_*127del, XM_047449543.1:c.*124_*127del, XM_047449543.1:c.*125_*127del, XM_047449543.1:c.*126_*127del, XM_047449543.1:c.*127del, XM_047449543.1:c.*127dup, XM_047449543.1:c.*126_*127dup, XM_047449543.1:c.*125_*127dup, XM_047449543.1:c.*124_*127dup, XM_047449543.1:c.*123_*127dup, XM_047449543.1:c.*122_*127dup, XM_047449543.1:c.*121_*127dup, XM_047449543.1:c.*120_*127dup, XM_047449543.1:c.*119_*127dup, XM_047449543.1:c.*118_*127dup, XM_047449543.1:c.*117_*127dup, XM_047449543.1:c.*115_*127dup, XM_047449543.1:c.*114_*127dup, XM_047449543.1:c.*127_*128insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

    2.

    rs1491081726 has merged into rs71204079 [Homo sapiens]
      Variant type:
      DELINS
      Alleles:
      AA>-,A,AAA,AAAA [Show Flanks]
      Chromosome:
      4:69206302 (GRCh38)
      4:70072020 (GRCh37)
      Canonical SPDI:
      NC_000004.12:69206295:AAAAAAAA:AAAAAA,NC_000004.12:69206295:AAAAAAAA:AAAAAAA,NC_000004.12:69206295:AAAAAAAA:AAAAAAAAA,NC_000004.12:69206295:AAAAAAAA:AAAAAAAAAA
      Gene:
      UGT2B11 (Varview), LOC105377267 (Varview)
      Functional Consequence:
      intron_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      AAAAAAAAAA=0./0 (ALFA)
      -=0.338/1596 (1000Genomes)
      HGVS:

      3.

      rs1491072318 has merged into rs377302567 [Homo sapiens]
        Variant type:
        DELINS
        Alleles:
        AA>-,A,AAA [Show Flanks]
        Chromosome:
        4:69200311 (GRCh38)
        4:70066029 (GRCh37)
        Canonical SPDI:
        NC_000004.12:69200308:AAAA:AA,NC_000004.12:69200308:AAAA:AAA,NC_000004.12:69200308:AAAA:AAAAA
        Gene:
        UGT2B11 (Varview), LOC105377267 (Varview)
        Functional Consequence:
        intron_variant,3_prime_UTR_variant
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        AAAAA=0./0 (ALFA)
        -=0.000004/1 (TOPMED)
        -=0.04476/82 (Korea1K)
        -=0.058333/35 (NorthernSweden)
        -=0.066132/66 (GoNL)
        -=0.084053/1408 (TOMMO)
        HGVS:

        4.

        rs1491051364 [Homo sapiens]
          Variant type:
          DEL
          Alleles:
          AC>- [Show Flanks]
          Chromosome:
          4:69209584 (GRCh38)
          4:70075302 (GRCh37)
          Canonical SPDI:
          NC_000004.12:69209583:AC:
          Gene:
          UGT2B11 (Varview), LOC105377267 (Varview)
          Functional Consequence:
          intron_variant
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          -=0./0 (ALFA)
          -=0.000007/1 (GnomAD)
          -=0.000015/4 (TOPMED)
          -=0.000142/2 (TOMMO)
          HGVS:

          5.

          rs1490889173 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            T>C [Show Flanks]
            Chromosome:
            4:69201334 (GRCh38)
            4:70067052 (GRCh37)
            Canonical SPDI:
            NC_000004.12:69201333:T:C
            Gene:
            UGT2B11 (Varview), LOC105377267 (Varview)
            Functional Consequence:
            intron_variant
            Validated:
            by frequency,by alfa,by cluster
            MAF:
            C=0./0 (ALFA)
            C=0.000008/2 (TOPMED)
            C=0.000036/5 (GnomAD)
            HGVS:

            6.

            rs1490877466 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              T>G [Show Flanks]
              Chromosome:
              4:69214179 (GRCh38)
              4:70079897 (GRCh37)
              Canonical SPDI:
              NC_000004.12:69214178:T:G
              Gene:
              UGT2B11 (Varview), LOC105377267 (Varview)
              Functional Consequence:
              intron_variant,coding_sequence_variant,synonymous_variant
              Validated:
              by frequency
              MAF:
              G=0.000004/1 (GnomAD_exomes)
              HGVS:

              7.

              rs1490819673 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                A>T [Show Flanks]
                Chromosome:
                4:69223932 (GRCh38)
                4:70089650 (GRCh37)
                Canonical SPDI:
                NC_000004.12:69223931:A:T
                Gene:
                UGT2B11 (Varview)
                Functional Consequence:
                intron_variant,genic_upstream_transcript_variant
                Validated:
                by frequency,by alfa,by cluster
                MAF:
                T=0.000071/1 (ALFA)
                T=0.000019/5 (TOPMED)
                T=0.000035/1 (TOMMO)
                T=0.00005/7 (GnomAD)
                HGVS:

                8.

                rs1490681244 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  G>T [Show Flanks]
                  Chromosome:
                  4:69201465 (GRCh38)
                  4:70067183 (GRCh37)
                  Canonical SPDI:
                  NC_000004.12:69201464:G:T
                  Gene:
                  UGT2B11 (Varview), LOC105377267 (Varview)
                  Functional Consequence:
                  intron_variant
                  Validated:
                  by frequency,by alfa
                  MAF:
                  T=0.000071/1 (ALFA)
                  T=0.000004/1 (TOPMED)
                  HGVS:

                  9.

                  rs1490518594 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    A>G [Show Flanks]
                    Chromosome:
                    4:69225375 (GRCh38)
                    4:70091093 (GRCh37)
                    Canonical SPDI:
                    NC_000004.12:69225374:A:G
                    Gene:
                    UGT2B11 (Varview)
                    Functional Consequence:
                    upstream_transcript_variant,2KB_upstream_variant
                    Validated:
                    by frequency,by alfa,by cluster
                    MAF:
                    G=0./0 (ALFA)
                    G=0.000021/3 (GnomAD)
                    HGVS:

                    10.

                    rs1490516447 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      A>C [Show Flanks]
                      Chromosome:
                      4:69201826 (GRCh38)
                      4:70067544 (GRCh37)
                      Canonical SPDI:
                      NC_000004.12:69201825:A:C
                      Gene:
                      UGT2B11 (Varview), LOC105377267 (Varview)
                      Functional Consequence:
                      intron_variant
                      Validated:
                      by frequency,by alfa
                      MAF:
                      C=0./0 (ALFA)
                      C=0.000008/2 (TOPMED)
                      HGVS:

                      11.

                      rs1490370728 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        A>G [Show Flanks]
                        Chromosome:
                        4:69213175 (GRCh38)
                        4:70078893 (GRCh37)
                        Canonical SPDI:
                        NC_000004.12:69213174:A:G
                        Gene:
                        UGT2B11 (Varview), LOC105377267 (Varview)
                        Functional Consequence:
                        intron_variant
                        Validated:
                        by frequency,by alfa,by cluster
                        MAF:
                        G=0./0 (ALFA)
                        G=0.000011/3 (TOPMED)
                        G=0.000014/2 (GnomAD)
                        HGVS:

                        12.

                        rs1490330283 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          G>A,C [Show Flanks]
                          Chromosome:
                          4:69221613 (GRCh38)
                          4:70087331 (GRCh37)
                          Canonical SPDI:
                          NC_000004.12:69221612:G:A,NC_000004.12:69221612:G:C
                          Gene:
                          UGT2B11 (Varview)
                          Functional Consequence:
                          intron_variant,genic_upstream_transcript_variant
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          C=0./0 (ALFA)
                          C=0.000015/4 (TOPMED)
                          A=0.000685/2 (KOREAN)
                          HGVS:

                          13.

                          rs1490327808 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            C>T [Show Flanks]
                            Chromosome:
                            4:69211603 (GRCh38)
                            4:70077321 (GRCh37)
                            Canonical SPDI:
                            NC_000004.12:69211602:C:T
                            Gene:
                            UGT2B11 (Varview), LOC105377267 (Varview)
                            Functional Consequence:
                            intron_variant
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            T=0.000142/2 (ALFA)
                            T=0.000029/4 (GnomAD)
                            T=0.000057/15 (TOPMED)
                            HGVS:

                            14.

                            rs1490304374 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              T>C [Show Flanks]
                              Chromosome:
                              4:69222191 (GRCh38)
                              4:70087909 (GRCh37)
                              Canonical SPDI:
                              NC_000004.12:69222190:T:C
                              Gene:
                              UGT2B11 (Varview)
                              Functional Consequence:
                              intron_variant,genic_upstream_transcript_variant
                              Validated:
                              by frequency,by alfa
                              MAF:
                              C=0./0 (ALFA)
                              HGVS:

                              15.

                              rs1490225240 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                C>T [Show Flanks]
                                Chromosome:
                                4:69211355 (GRCh38)
                                4:70077073 (GRCh37)
                                Canonical SPDI:
                                NC_000004.12:69211354:C:T
                                Gene:
                                UGT2B11 (Varview), LOC105377267 (Varview)
                                Functional Consequence:
                                intron_variant
                                Validated:
                                by frequency,by alfa
                                MAF:
                                T=0./0 (ALFA)
                                T=0.000014/2 (GnomAD)
                                HGVS:

                                16.

                                rs1490096650 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  G>A [Show Flanks]
                                  Chromosome:
                                  4:69213227 (GRCh38)
                                  4:70078945 (GRCh37)
                                  Canonical SPDI:
                                  NC_000004.12:69213226:G:A
                                  Gene:
                                  UGT2B11 (Varview), LOC105377267 (Varview)
                                  Functional Consequence:
                                  intron_variant
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  A=0.000071/1 (ALFA)
                                  A=0.000004/1 (TOPMED)
                                  A=0.000007/1 (GnomAD)
                                  HGVS:

                                  17.

                                  rs1490077418 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    A>G [Show Flanks]
                                    Chromosome:
                                    4:69216564 (GRCh38)
                                    4:70082282 (GRCh37)
                                    Canonical SPDI:
                                    NC_000004.12:69216563:A:G
                                    Gene:
                                    UGT2B11 (Varview), LOC105377267 (Varview)
                                    Functional Consequence:
                                    intron_variant,upstream_transcript_variant,non_coding_transcript_variant,genic_upstream_transcript_variant
                                    Validated:
                                    by frequency,by alfa,by cluster
                                    MAF:
                                    G=0./0 (ALFA)
                                    G=0.000007/1 (GnomAD)
                                    G=0.000008/2 (TOPMED)
                                    HGVS:

                                    18.

                                    rs1489975929 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      T>G [Show Flanks]
                                      Chromosome:
                                      4:69200825 (GRCh38)
                                      4:70066543 (GRCh37)
                                      Canonical SPDI:
                                      NC_000004.12:69200824:T:G
                                      Gene:
                                      UGT2B11 (Varview), LOC105377267 (Varview)
                                      Functional Consequence:
                                      intron_variant
                                      Validated:
                                      by frequency,by alfa
                                      MAF:
                                      G=0./0 (ALFA)
                                      G=0.000004/1 (TOPMED)
                                      HGVS:

                                      19.

                                      rs1489885764 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        C>T [Show Flanks]
                                        Chromosome:
                                        4:69224493 (GRCh38)
                                        4:70090211 (GRCh37)
                                        Canonical SPDI:
                                        NC_000004.12:69224492:C:T
                                        Gene:
                                        UGT2B11 (Varview)
                                        Functional Consequence:
                                        intron_variant,genic_upstream_transcript_variant
                                        HGVS:

                                        20.

                                        rs1489856540 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          G>A [Show Flanks]
                                          Chromosome:
                                          4:69206214 (GRCh38)
                                          4:70071932 (GRCh37)
                                          Canonical SPDI:
                                          NC_000004.12:69206213:G:A
                                          Gene:
                                          UGT2B11 (Varview), LOC105377267 (Varview)
                                          Functional Consequence:
                                          intron_variant
                                          Validated:
                                          by frequency,by alfa
                                          MAF:
                                          A=0./0 (ALFA)
                                          A=0.000004/1 (TOPMED)
                                          HGVS:

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