Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 78
rs121434568 0.568 0.560 7 55191822 missense variant T/A;G snv 73
rs1057519847 0.570 0.560 7 55191821 missense variant CT/AG mnv 72
rs1057519848 0.570 0.560 7 55191822 missense variant TG/GT mnv 72
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 57
rs1412125 0.724 0.360 13 30467458 intron variant C/G;T snv 17
rs1360485 0.742 0.320 13 30457747 3 prime UTR variant C/T snv 0.58 16
rs765433422 0.807 0.160 10 87952250 stop gained G/A;T snv 8.0E-06 7.0E-06 7
rs564064363 0.851 0.080 17 39706998 missense variant G/A;C snv 1.3E-05 4