Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs5186 0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35
rs1801253 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 34
rs8192678 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 28
rs4961 0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 27
rs5219 0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 25
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 24
rs10719 0.677 0.680 5 31401340 3 prime UTR variant A/G;T snv 0.69 24
rs660339 0.695 0.320 11 73978059 missense variant G/A snv 0.41 0.43 24
rs762551 0.701 0.400 15 74749576 intron variant C/A snv 0.67 23
rs11556924 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 21
rs2228611 0.708 0.520 19 10156401 synonymous variant T/A;C snv 0.52 19
rs1043210477 0.701 0.520 3 49358250 missense variant G/A snv 19
rs1065852 0.695 0.360 22 42130692 missense variant G/A snv 0.21 0.19 19
rs4244285 0.695 0.360 10 94781859 synonymous variant G/A;C snv 0.18 18
rs2071746 0.708 0.320 22 35380679 intron variant A/T snv 0.49 18
rs10046 0.708 0.400 15 51210789 3 prime UTR variant G/A snv 0.45 0.43 18
rs11053646 0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13 18
rs1801252 0.724 0.320 10 114044277 missense variant A/G snv 0.15 0.17 17
rs659366 0.724 0.520 11 73983709 non coding transcript exon variant C/T snv 0.40 17
rs5751876 0.742 0.320 22 24441333 synonymous variant T/C snv 0.54 0.52 16
rs5182 0.742 0.160 3 148741608 synonymous variant C/T snv 0.49 0.41 16
rs751141 0.732 0.400 8 27516348 missense variant G/A snv 0.12 0.10 16
rs713041 0.776 0.400 19 1106616 stop gained T/A;C snv 4.2E-06; 0.58 16