Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs77375493 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 59
rs1800566 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs759412116 0.581 0.640 19 45352210 missense variant C/G;T snv 4.0E-06; 6.0E-05 55
rs9344 0.653 0.480 11 69648142 splice region variant G/A snv 0.45 0.39 34
rs1057520007 0.701 0.440 17 7674917 missense variant T/A;C;G snv 21