Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519786 0.882 0.160 X 47566722 missense variant C/G;T snv 3
rs1057519876 0.882 0.160 X 47566721 missense variant T/G snv 3
rs1023835002 0.763 0.280 15 44711547 start lost A/G;T snv 10
rs1057519877 0.763 0.280 15 44711549 start lost G/A snv 10
rs121913355 0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 32
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 22
rs121913364 0.641 0.520 7 140753334 missense variant T/C;G snv 4.0E-06 14
rs121913338 0.677 0.400 7 140753354 missense variant T/A;C;G snv 12
rs121913357 0.742 0.320 7 140781603 stop gained C/A;G;T snv 11
rs397516896 0.763 0.360 7 140753355 missense variant C/G;T snv 11
rs397507484 0.752 0.480 7 140753333 missense variant T/A;C;G snv 10
rs121913351 0.776 0.240 7 140781611 missense variant C/A;G;T snv 4.0E-06 9
rs121913370 0.763 0.360 7 140753393 missense variant T/C;G snv 9
rs180177040 0.790 0.360 7 140754187 missense variant T/C;G snv 9
rs121913365 0.776 0.320 7 140753332 missense variant T/A;G snv 8
rs121913366 0.763 0.400 7 140753345 missense variant A/C;T snv 6
rs121913378 0.776 0.280 7 140753337 missense variant C/A;G;T snv 6
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 2
rs121913227 0.653 0.320 7 140753336 missense variant AC/CT;TT mnv 1
rs1057519918 0.851 0.200 8 127738390 missense variant C/T snv 5
rs750664148 0.851 0.200 8 127738434 missense variant A/C;G snv 5
rs11547328 0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06 6
rs104894340 0.827 0.200 12 57751647 missense variant C/A;T snv 5
rs1057519883 0.742 0.280 9 21971120 missense variant C/G;T snv 11
rs34968276 0.776 0.240 9 21971110 stop gained G/A;C;T snv 9