Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs334
HBB
0.724 0.240 11 5227002 missense variant T/A;C;G snv 3.5E-03 35
rs5744680 0.851 0.120 5 75584065 intron variant G/A snv 0.55 18
rs1050828 0.790 0.200 X 154536002 missense variant C/T snv 9.1E-03 3.6E-02 15