Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913355 0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 32
rs28934574 0.658 0.440 17 7673776 missense variant G/A;C snv 4.0E-06 27
rs28934573 0.667 0.480 17 7674241 missense variant G/A;C;T snv 4.0E-06 24
rs730882008 0.683 0.440 17 7673775 missense variant C/A;G;T snv 4.0E-06 22
rs1057520002 0.695 0.360 17 7674242 missense variant A/C;G snv 20
rs1057519942 0.724 0.320 3 179203760 missense variant G/A snv 15
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
rs121913338 0.677 0.400 7 140753354 missense variant T/A;C;G snv 12
rs121913357 0.742 0.320 7 140781603 stop gained C/A;G;T snv 11
rs1023835002 0.763 0.280 15 44711547 start lost A/G;T snv 10
rs1057519877 0.763 0.280 15 44711549 start lost G/A snv 10
rs1057519879 0.763 0.280 15 44711548 start lost T/C;G snv 10
rs1057519941 0.776 0.240 3 179203761 missense variant T/C;G snv 9
rs869025608 0.763 0.400 15 66435117 missense variant G/C;T snv 9
rs1057519909 0.790 0.240 15 66435116 missense variant A/C snv 6
rs756091827 0.851 0.200 8 127738435 missense variant C/G;T snv 6
rs1057519918 0.851 0.200 8 127738390 missense variant C/T snv 5
rs750664148 0.851 0.200 8 127738434 missense variant A/C;G snv 5
rs267601394 0.807 0.200 7 148811635 missense variant T/A;G snv 3
rs267601395 0.925 0.160 7 148811636 missense variant A/G;T snv 3
rs1057519894 0.925 0.160 7 148811650 missense variant T/A;G snv 2