Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 6
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
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 48
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 39
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 35
rs104894229 0.564 0.600 11 534289 missense variant C/A;G;T snv 52
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
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 42
rs121912651 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 37
rs104894228 0.605 0.560 11 534286 missense variant C/A;G;T snv 30
rs121913273 0.605 0.440 3 179218294 missense variant G/A;C snv 25
rs121913343 0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 29
rs121913237 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 12
rs79184941 0.617 0.600 10 121520163 missense variant G/A;C snv 5.6E-05; 4.0E-06 18
rs2274223 0.620 0.400 10 94306584 missense variant A/G snv 0.28 0.31 4
rs121913281 0.623 0.520 3 179234296 missense variant C/T snv 37
rs121909224 0.627 0.560 10 87933147 stop gained C/G;T snv 1.2E-05 35
rs121913233 0.627 0.520 11 533874 missense variant T/A;C;G snv 21
rs397516436 0.641 0.440 17 7674894 stop gained G/A;C snv 26
rs28934575 0.641 0.400 17 7674230 missense variant C/A;G;T snv 25
rs121913364 0.641 0.520 7 140753334 missense variant T/C;G snv 4.0E-06 14
rs886039484 0.641 0.440 17 7674888 missense variant T/C;G snv 10
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 30