Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 1
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 1
rs121913338 0.677 0.400 7 140753354 missense variant T/A;C;G snv 1
rs121913351 0.776 0.240 7 140781611 missense variant C/A;G;T snv 4.0E-06 2
rs1057519895 0.724 0.240 4 152328232 missense variant C/A;G;T snv 1
rs1057519922 0.790 0.200 2 177234082 missense variant C/G;T snv 1
rs1057519929 0.776 0.320 3 179199066 missense variant G/A snv 1
rs121913287 0.752 0.400 3 179199088 missense variant G/A snv 1
rs587777790 0.732 0.280 3 179199690 missense variant G/A snv 1
rs1057519925 0.683 0.560 3 179210291 missense variant G/A;C snv 1
rs121913273 0.605 0.440 3 179218294 missense variant G/A;C snv 5
rs1057519927 0.716 0.240 3 179218295 missense variant A/C;G;T snv 1
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 4
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 3
rs121913286 0.677 0.280 3 179218306 missense variant C/A;G snv 2
rs397517201 0.732 0.240 3 179218307 missense variant A/C;G;T snv 1
rs867262025 0.790 0.360 3 179221146 missense variant G/A snv 1
rs121913283 0.724 0.440 3 179234286 missense variant G/A;T snv 4.0E-06 2
rs121913281 0.623 0.520 3 179234296 missense variant C/T snv 1
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 7
rs121913482 0.630 0.680 4 1801837 missense variant C/T snv 4
rs121913483 0.649 0.560 4 1801841 missense variant C/A;G;T snv 4.2E-06; 1.3E-05 4
rs121913386 0.807 0.120 9 21971018 missense variant G/A;T snv 1
rs121913385 0.763 0.240 9 21971112 missense variant G/A;C snv 1
rs1057519883 0.742 0.280 9 21971120 missense variant C/G;T snv 1