Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3131378 0.925 0.200 6 31757508 non coding transcript exon variant A/G snv 7.9E-02 2
rs11137037 0.851 0.200 8 6538661 intron variant A/C snv 0.40 4
rs12674822 0.851 0.200 8 6531695 intron variant T/G snv 0.49 4
rs12901682 0.851 0.200 15 78540881 5 prime UTR variant A/C;T snv 4
rs2281089 0.851 0.200 22 37136132 intron variant A/G snv 0.17 4
rs3115672 0.851 0.200 6 31760120 synonymous variant C/T snv 6.4E-02 7.9E-02 4
rs7383287 0.851 0.320 6 32815309 synonymous variant A/G snv 0.18 0.19 4
rs791588 0.851 0.200 10 6047379 intron variant G/T snv 0.40 4
rs969129 0.851 0.200 5 35861166 intron variant T/A;G snv 4
rs2847297 0.827 0.200 18 12797695 intron variant A/G snv 0.40 5
rs2929970 0.827 0.200 8 133228894 3 prime UTR variant G/A snv 0.52 5
rs2929973 0.851 0.200 8 133230265 3 prime UTR variant G/T snv 0.85 5
rs11543848 0.790 0.240 7 55161562 missense variant G/A;C;T snv 7
rs2075786 0.790 0.360 5 1266195 intron variant A/G snv 0.55 8
rs3817963 0.776 0.360 6 32400310 intron variant T/C snv 0.25 8
rs62514004 0.790 0.240 8 133190246 upstream gene variant A/G snv 0.28 8
rs140693 0.763 0.280 3 129436608 missense variant C/T snv 5.8E-02 3.1E-02 10
rs3219175 0.807 0.240 19 7668969 upstream gene variant G/A snv 5.0E-02 10
rs1535045 0.742 0.360 20 46119460 intron variant C/A;G;T snv 12
rs3117582 0.716 0.440 6 31652743 intron variant T/G snv 7.1E-02 14
rs1360485 0.742 0.320 13 30457747 3 prime UTR variant C/T snv 0.58 16
rs1412125 0.724 0.360 13 30467458 intron variant C/G;T snv 17
rs1799930 0.716 0.400 8 18400593 missense variant G/A snv 0.27 0.27 17
rs2395185 0.724 0.360 6 32465390 intron variant G/T snv 0.29 17
rs767649 0.695 0.480 21 25572410 intron variant T/A snv 7.5E-02 18