Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 36
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 28
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 25
rs121913255 0.667 0.400 1 114713907 missense variant T/A;G snv 19
rs121913364 0.641 0.520 7 140753334 missense variant T/C;G snv 4.0E-06 14
rs28931588 0.701 0.200 3 41224606 missense variant G/A;C;T snv 14
rs121913403 0.683 0.240 3 41224622 missense variant C/A;G;T snv 13
rs28931589 0.695 0.240 3 41224613 missense variant G/A;C;T snv 13
rs121913237 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 12
rs121913250 0.683 0.440 1 114716127 missense variant C/A;G;T snv 12
rs121913396 0.732 0.200 3 41224607 missense variant A/C;G;T snv 11
rs121913407 0.763 0.240 3 41224645 missense variant T/C;G snv 10
rs397507484 0.752 0.480 7 140753333 missense variant T/A;C;G snv 10
rs121913409 0.708 0.400 3 41224646 missense variant C/A;G;T snv 9
rs121913365 0.776 0.320 7 140753332 missense variant T/A;G snv 8
rs1057519732 0.827 0.160 15 66436824 missense variant C/A;T snv 6
rs397516792 0.827 0.280 15 66436825 missense variant C/A;G;T snv 6