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
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 96
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
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs121912651 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 53
rs17879961 0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 53
rs104894228 0.605 0.560 11 534286 missense variant C/A;G;T snv 48
rs121912664 0.630 0.320 17 7670699 missense variant C/A;G;T snv 1.2E-05 44
rs1057519975 0.649 0.480 17 7675209 missense variant A/C;G;T snv 34
rs1136201 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 34
rs760043106 0.645 0.440 17 7674947 missense variant A/C;G;T snv 32
rs6505162 0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05 25
rs1057519816 0.763 0.200 17 39711955 missense variant C/A;T snv 14
rs1213469537 0.882 0.080 7 116559145 missense variant C/T snv 4.0E-06 1.4E-05 9
rs62625308 0.851 0.200 17 43091924 stop gained G/A;C snv 1.2E-05 8