Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs1057519927 0.716 0.240 3 179218295 missense variant A/C;G;T snv 19
rs1057519975 0.649 0.480 17 7675209 missense variant A/C;G;T snv 34
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 33
rs121913396 0.732 0.200 3 41224607 missense variant A/C;G;T snv 13
rs397517201 0.732 0.240 3 179218307 missense variant A/C;G;T snv 16
rs530941076 0.695 0.280 17 7674873 missense variant A/C;G;T snv 4.0E-06 21
rs864622237 0.716 0.320 17 7674263 missense variant A/C;G;T snv 17
rs967461896 0.724 0.240 17 7675086 missense variant A/C;G;T snv 17
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs121913286 0.677 0.280 3 179218306 missense variant C/A;G snv 23
rs104894229 0.564 0.600 11 534289 missense variant C/A;G;T snv 73
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 57
rs121912656 0.662 0.560 17 7674229 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 28
rs121913355 0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 42
rs121913357 0.742 0.320 7 140781603 stop gained C/A;G;T snv 12
rs121913400 0.683 0.360 3 41224610 missense variant C/A;G;T snv 26
rs121913403 0.683 0.240 3 41224622 missense variant C/A;G;T snv 23
rs121913409 0.708 0.400 3 41224646 missense variant C/A;G;T snv 21
rs121913496 0.724 0.440 11 533873 missense variant C/A;G;T snv 16
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 96
rs28934575 0.641 0.400 17 7674230 missense variant C/A;G;T snv 37
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 78