Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 7
rs121913530 0.583 0.640 12 25245351 missense variant C/A;G;T snv 5
rs121913273 0.605 0.440 3 179218294 missense variant G/A;C snv 5
rs121913355 0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 4
rs121913400 0.683 0.360 3 41224610 missense variant C/A;G;T snv 4
rs121913482 0.630 0.680 4 1801837 missense variant C/T snv 4
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 4
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 4
rs121913403 0.683 0.240 3 41224622 missense variant C/A;G;T snv 3
rs121913413 0.763 0.240 3 41224634 missense variant C/A;T snv 3
rs77375493 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 3
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 3
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 3
rs121913351 0.776 0.240 7 140781611 missense variant C/A;G;T snv 4.0E-06 2
rs121913364 0.641 0.520 7 140753334 missense variant T/C;G snv 4.0E-06 2
rs121913228 0.742 0.200 3 41224621 missense variant T/C;G snv 2
rs121913495 0.672 0.400 20 58909366 missense variant G/A;T snv 2
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 2
rs121913499 0.605 0.520 2 208248389 missense variant G/A;C;T snv 2
rs104894228 0.605 0.560 11 534286 missense variant C/A;G;T snv 2
rs80338796 0.667 0.480 3 12604200 missense variant G/A;C snv 4.0E-06 2
rs121913315 0.882 0.160 19 1220488 missense variant G/A;T snv 2
rs121912666 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 2
rs863225281
ALK
0.776 0.200 2 29220829 missense variant G/C;T snv 1
rs879254046
ATM
0.925 0.240 11 108267246 stop gained G/A;C;T snv 1