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
rs121913273 0.605 0.440 3 179218294 missense variant G/A;C snv 5
rs121913400 0.683 0.360 3 41224610 missense variant C/A;G;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
rs121913272 0.752 0.400 3 179210192 missense variant T/C;G snv 3
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 3
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
rs121913396 0.732 0.200 3 41224607 missense variant A/C;G;T snv 2
rs28931588 0.701 0.200 3 41224606 missense variant G/A;C;T 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
rs104894228 0.605 0.560 11 534286 missense variant C/A;G;T snv 2
rs121434595 0.708 0.320 1 114716124 missense variant C/A;G;T snv 2
rs121434596 0.677 0.440 1 114716123 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 2
rs121913237 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 2
rs121913283 0.724 0.440 3 179234286 missense variant G/A;T snv 4.0E-06 2
rs121913286 0.677 0.280 3 179218306 missense variant C/A;G snv 2
rs80338796 0.667 0.480 3 12604200 missense variant G/A;C snv 4.0E-06 2
rs121912666 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 2
rs764255410 1.000 0.080 2 147918546 missense variant G/A snv 1
rs566841339 1.000 0.080 2 219489128 missense variant G/A snv 2.8E-05 2.8E-05 1
rs747576071
AXL
1.000 0.080 19 41243665 missense variant C/T snv 1.6E-05 7.0E-06 1