Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913255 0.667 0.400 1 114713907 missense variant T/A;G snv 19
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 25
rs121434596 0.677 0.440 1 114716123 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 14
rs121434595 0.708 0.320 1 114716124 missense variant C/A;G;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
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 22
rs121913366 0.763 0.400 7 140753345 missense variant A/C;T snv 6
rs121913338 0.677 0.400 7 140753354 missense variant T/A;C;G snv 12
rs397516896 0.763 0.360 7 140753355 missense variant C/G;T snv 11
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
rs121913355 0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 32
rs121913357 0.742 0.320 7 140781603 stop gained C/A;G;T snv 11
rs121913351 0.776 0.240 7 140781611 missense variant C/A;G;T snv 4.0E-06 9
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 18
rs121913499 0.605 0.520 2 208248389 missense variant G/A;C;T snv 16
rs770248150 0.807 0.240 12 25225713 missense variant T/A;G snv 4.0E-06 6
rs17851045 0.672 0.400 12 25227341 missense variant T/A;G snv 4.0E-06 15
rs1023835002 0.763 0.280 15 44711547 start lost A/G;T snv 10
rs1057519879 0.763 0.280 15 44711548 start lost T/C;G snv 10
rs1057519877 0.763 0.280 15 44711549 start lost G/A snv 10
rs121913233 0.627 0.520 11 533874 missense variant T/A;C;G snv 20
rs28933406 0.667 0.480 11 533875 missense variant G/C;T snv 17
rs104894226 0.658 0.560 11 534285 missense variant C/A;G;T snv 23