Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs79204362 0.763 0.120 2 38071251 missense variant C/T snv 5.8E-03 1.7E-03 2
rs74315339 0.807 0.120 1 171652468 missense variant C/A snv 9.8E-04 1.3E-04 2
rs199746824 0.807 0.040 1 171652139 missense variant C/G;T snv 4.0E-06; 1.6E-05 1
rs200120115 1.000 0.040 1 171652236 missense variant G/A snv 1.5E-04 1.3E-04 1
rs200208925 0.925 0.040 1 171652454 missense variant A/G snv 6.4E-05 2.1E-05 1
rs755246983 0.925 0.040 1 171652539 missense variant A/G snv 8.0E-06; 4.0E-06 1
rs764005392 1.000 0.040 1 171652368 missense variant G/A snv 7.6E-05 7.7E-05 1
rs1200513428 1.000 0.040 1 171636140 missense variant C/T snv 4.0E-06 1
rs121909194 0.882 0.040 1 171636302 missense variant C/G snv 1
rs1344039930 1.000 0.040 1 171636359 missense variant G/A snv 7.0E-06 1
rs1351328951 1.000 0.040 1 171636584 missense variant A/G snv 8.0E-06 1
rs137853277 0.925 0.040 1 171636382 missense variant G/A snv 7.0E-04 3.1E-04 1
rs139122673 1.000 0.040 1 171636562 missense variant G/A;T snv 1.2E-05; 5.9E-04 1
rs201573718 1.000 0.040 1 171636175 missense variant C/T snv 2.4E-05 5.6E-05 1
rs28936694 0.925 0.040 1 171636244 missense variant C/A snv 1.6E-05 1
rs61745146 1.000 0.040 1 171636386 missense variant C/G;T snv 9.3E-04 1
rs74315328 0.807 0.120 1 171636131 missense variant A/G snv 1
rs74315331 0.882 0.040 1 171636010 missense variant A/C;T snv 1
rs74315338 0.882 0.040 1 171636143 missense variant A/G snv 1
rs74315340 1.000 0.040 1 171636706 missense variant C/T snv 1
rs74315341 0.851 0.040 1 171636686 missense variant C/T snv 1
rs748621461 0.925 0.040 1 171636542 missense variant C/T snv 3.2E-05 2.1E-05 1
rs754237376 0.882 0.080 1 171636161 missense variant C/T snv 4.8E-05 2.1E-05 1
rs757769997 1.000 0.040 1 171636709 missense variant C/A snv 2.5E-05 7.0E-06 1
rs771122834 1.000 0.040 1 171636032 missense variant G/A snv 2.0E-05 1.4E-05 1