Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs1799971 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs1718125 0.851 0.200 12 121155216 intron variant C/T snv 0.15 0.19 6
rs373611092 0.925 0.160 22 19962794 missense variant A/G snv 8.4E-05 4.9E-05 5