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
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 78
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs104894229 0.564 0.600 11 534289 missense variant C/A;G;T snv 73
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 59
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 57
rs121912651 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 53
rs121913237 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 50
rs104894228 0.605 0.560 11 534286 missense variant C/A;G;T snv 48
rs121913273 0.605 0.440 3 179218294 missense variant G/A;C snv 44
rs121913343 0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 44
rs79184941 0.617 0.600 10 121520163 missense variant G/A;C snv 5.6E-05; 4.0E-06 41
rs121909224 0.627 0.560 10 87933147 stop gained C/G;T snv 1.2E-05 41
rs2274223 0.620 0.400 10 94306584 missense variant A/G snv 0.28 0.31 40
rs121913233 0.627 0.520 11 533874 missense variant T/A;C;G snv 37
rs121913281 0.623 0.520 3 179234296 missense variant C/T snv 37
rs80338796 0.667 0.480 3 12604200 missense variant G/A;C snv 4.0E-06 37
rs28934575 0.641 0.400 17 7674230 missense variant C/A;G;T snv 37