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
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
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
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 78
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 57
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs17879961 0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 53
rs2273535 0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 38
rs752742313 0.637 0.320 3 138655502 missense variant C/T snv 1.2E-05 36
rs1057519975 0.649 0.480 17 7675209 missense variant A/C;G;T snv 34
rs760043106 0.645 0.440 17 7674947 missense variant A/C;G;T snv 32
rs886039484 0.641 0.440 17 7674888 missense variant T/C;G snv 32
rs1058808 0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 27
rs3803662 0.662 0.440 16 52552429 non coding transcript exon variant A/G snv 0.63 25
rs6505162 0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05 25
rs483352697 0.695 0.480 17 7674944 missense variant C/A;G;T snv 4.0E-06 21
rs1273593548 0.716 0.160 7 106867593 missense variant T/G snv 8.4E-06 19
rs587781991 0.724 0.240 17 7675208 missense variant C/A;T snv 17