Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519932 0.683 0.320 3 179234298 missense variant T/G snv 22
rs1057519999 0.763 0.160 17 7674247 missense variant T/C;G snv 12
rs121912666 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 24
rs587780073 0.708 0.400 17 7674262 missense variant T/C;G snv 17
rs730882026 0.742 0.440 17 7674256 missense variant T/C;G snv 12
rs876660807 0.763 0.160 17 7674248 missense variant T/C snv 12
rs121913284 0.776 0.160 3 179203765 missense variant T/A;G snv 10
rs121913233 0.627 0.520 11 533874 missense variant T/A;C;G snv 20
rs786201838 0.683 0.440 17 7674953 missense variant T/A;C;G snv 23
rs1057519940 0.752 0.200 3 179218308 missense variant G/T snv 13
rs869025608 0.763 0.400 15 66435117 missense variant G/C;T snv 9
rs1057519977 0.763 0.360 17 7675189 missense variant G/C snv 13
rs121909229 0.683 0.400 10 87933148 missense variant G/A;C;T snv 23
rs121913275 0.672 0.320 3 179218305 missense variant G/A;C;T snv 4.0E-06 25
rs121913343 0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 29
rs876658468 0.689 0.440 17 7674954 missense variant G/A;C;T snv 22
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 34
rs121912651 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 37
rs121913273 0.605 0.440 3 179218294 missense variant G/A;C snv 21
rs138729528 0.677 0.480 17 7675089 missense variant G/A;C snv 1.6E-05 25
rs28934574 0.658 0.440 17 7673776 missense variant G/A;C snv 4.0E-06 27
rs397516436 0.641 0.440 17 7674894 stop gained G/A;C snv 26
rs1057519947 0.790 0.160 19 52212730 missense variant G/A snv 9
rs121913287 0.752 0.400 3 179199088 missense variant G/A snv 11
rs587777790 0.732 0.280 3 179199690 missense variant G/A snv 12