Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs78378222 0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 37
rs1047891 0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 34
rs7705526 0.776 0.240 5 1285859 intron variant C/A;T snv 15
rs13331259 16 249924 intron variant A/G snv 3.0E-02 14
rs7385804 0.851 0.120 7 100638347 intron variant C/A snv 0.65 14
rs35188965 5 1104823 intron variant C/G;T snv 12
rs3811444 1 247876149 missense variant C/T snv 0.31 0.26 12
rs2179593 0.790 0.080 20 44031646 intron variant C/A snv 0.71 11
rs17758695 18 63253621 intron variant C/T snv 2.1E-02 10
rs218265 4 54542832 intergenic variant T/C snv 0.21 10
rs4895441 0.925 0.080 6 135105435 upstream gene variant A/G snv 0.21 10
rs9487023 6 109268801 intron variant A/G snv 0.40 8
rs11970772 6 41957552 intron variant T/A snv 0.24 5
rs4449583 5 1284020 intron variant C/T snv 0.25 5
rs55709272 2 113109711 intron variant T/A;C snv 5
rs7955734 12 4223993 intergenic variant C/G snv 0.22 5
rs9804550 11 5164863 intergenic variant T/A;C snv 5
rs11211480 1 47227548 non coding transcript exon variant A/G snv 0.42 4
rs16928078 11 2298783 intron variant C/T snv 0.15 4
rs5756506 22 37071352 intron variant G/A;C snv 4
rs11190134 10 99522443 upstream gene variant G/A snv 0.36 3
rs139974673 15 43735687 intron variant T/C snv 2.0E-02 2
rs1977080 22 43934151 intron variant C/T snv 0.19 2
rs7803075 7 131057307 intron variant A/G snv 0.50 2