Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs752298579 0.701 0.480 22 20061538 missense variant G/A snv 1.4E-04 7.0E-06 48
rs1557043622 0.695 0.400 X 48909843 missense variant C/A snv 46
rs867410737 0.708 0.440 19 1242559 missense variant C/T snv 6.7E-06 45
rs587782995 0.708 0.360 5 140114480 missense variant T/C snv 42
rs886039469 0.701 0.560 10 76891709 missense variant T/C snv 35
rs146539065 0.752 0.240 4 25145092 synonymous variant C/T snv 2.8E-05 4.2E-05 34
rs776969714 0.752 0.240 4 25145129 splice acceptor variant -/C delins 4.2E-05 34
rs112445441 0.658 0.400 12 25245347 missense variant C/A;G;T snv 32
rs5219 0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 25
rs28936375 0.752 0.320 1 53197092 missense variant C/A snv 1.7E-04 2.2E-04 15
rs4149117 0.763 0.360 12 20858546 missense variant T/C;G snv 0.81 15
rs757075712 0.763 0.200 10 58390856 missense variant C/T snv 1.6E-05 1.4E-05 15
rs387906659 0.742 0.280 19 40257052 stop gained C/A;T snv 14
rs141322087 0.851 0.160 11 17404552 missense variant C/T snv 1.2E-05 2.1E-05 13
rs372949028 0.827 0.240 22 20061684 splice donor variant G/A;C snv 7.1E-05 5.6E-05 13
rs1344172059 0.882 0.080 11 17430838 missense variant C/T snv 7.0E-06 12
rs763028380 0.851 0.320 11 17453271 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 12
rs137852671 0.790 0.160 11 17394295 missense variant C/T snv 10
rs869025222 0.827 0.240 3 25580574 missense variant T/C snv 9
rs1799821 0.827 0.200 1 53210776 missense variant G/A snv 0.49 0.46 8
rs1801175 0.807 0.240 17 42903947 missense variant C/T snv 5.7E-04 3.4E-04 8
rs137853238 0.807 0.200 12 120994265 missense variant G/A snv 6
rs1272388614 0.851 0.080 11 17395658 missense variant C/T snv 2.4E-05 3.5E-05 5