Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 96
rs104894229 0.564 0.600 11 534289 missense variant C/A;G;T snv 73
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs121913530 0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs121913499 0.605 0.520 2 208248389 missense variant G/A;C;T snv 51
rs397516436 0.641 0.440 17 7674894 stop gained G/A;C snv 34
rs587778720 0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 31
rs121913272 0.752 0.400 3 179210192 missense variant T/C;G snv 13
rs121913284 0.776 0.160 3 179203765 missense variant T/A;G snv 11
rs121908390 0.807 0.200 16 50796443 stop gained C/G;T snv 4.0E-06 8