Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 5
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 4
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 6
rs121912651 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 37
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 42
rs104894229 0.564 0.600 11 534289 missense variant C/A;G;T snv 52
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 39
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 37
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 25
rs79184941 0.617 0.600 10 121520163 missense variant G/A;C snv 5.6E-05; 4.0E-06 18
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 48
rs121909224 0.627 0.560 10 87933147 stop gained C/G;T snv 1.2E-05 35
rs104894228 0.605 0.560 11 534286 missense variant C/A;G;T snv 30
rs1057519925 0.683 0.560 3 179210291 missense variant G/A;C snv 24
rs104894226 0.658 0.560 11 534285 missense variant C/A;G;T snv 23
rs121912656 0.662 0.560 17 7674229 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 20
rs121913237 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 12
rs121913281 0.623 0.520 3 179234296 missense variant C/T snv 37
rs121913343 0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 29
rs121913233 0.627 0.520 11 533874 missense variant T/A;C;G snv 21
rs121913364 0.641 0.520 7 140753334 missense variant T/C;G snv 4.0E-06 14
rs377767347 0.742 0.520 18 51065549 missense variant G/A;C;T snv 14
rs80338796 0.667 0.480 3 12604200 missense variant G/A;C snv 4.0E-06 35
rs138729528 0.677 0.480 17 7675089 missense variant G/A;C snv 1.6E-05 25
rs28934874 0.695 0.480 17 7675161 missense variant G/A;C;T snv 21