Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519917 0.807 0.160 1 11124517 missense variant A/G;T snv 7
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 25
rs121434595 0.708 0.320 1 114716124 missense variant C/A;G;T snv 13
rs121434596 0.677 0.440 1 114716123 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 14
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
rs121913255 0.667 0.400 1 114713907 missense variant T/A;G snv 19
rs587777894 0.776 0.240 1 11124516 missense variant G/A;T snv 9
rs121913499 0.605 0.520 2 208248389 missense variant G/A;C;T snv 16
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 18
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 34
rs1057519886 0.752 0.240 3 41224609 missense variant T/A;C;G snv 11
rs1057519932 0.683 0.320 3 179234298 missense variant T/G snv 22
rs1057519940 0.752 0.200 3 179218308 missense variant G/T snv 13
rs1057519941 0.776 0.240 3 179203761 missense variant T/C;G snv 9
rs1057519942 0.724 0.320 3 179203760 missense variant G/A snv 15
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 28
rs121913275 0.672 0.320 3 179218305 missense variant G/A;C;T snv 4.0E-06 25
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 45
rs121913281 0.623 0.520 3 179234296 missense variant C/T snv 37
rs121913286 0.677 0.280 3 179218306 missense variant C/A;G snv 20
rs121913400 0.683 0.360 3 41224610 missense variant C/A;G;T snv 17
rs121913407 0.763 0.240 3 41224645 missense variant T/C;G snv 10
rs121913409 0.708 0.400 3 41224646 missense variant C/A;G;T snv 9
rs121913412 0.724 0.280 3 41224633 missense variant A/C;G;T snv 10