Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10757274 0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs13058338 1.000 0.040 22 37236730 intron variant T/A;G snv 4
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs2070744 0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs2149954 0.882 0.080 5 158393594 intron variant C/T snv 0.37 5
rs2383206 0.742 0.320 9 22115027 intron variant A/G snv 0.49 17
rs2383207 0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs243866 0.827 0.120 16 55477625 intron variant G/A snv 0.19 8
rs6684209 1.000 0.040 1 115707991 intron variant C/T snv 0.17 2
rs9838915 0.882 0.120 3 126347377 intron variant G/A snv 0.19 4
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs5219 0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 25
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs10927887 0.925 0.040 1 16024780 missense variant A/C;G snv 0.55 3
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1303946678 0.925 0.040 22 42126851 missense variant C/G snv 3
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1800888 0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 23
rs1801252 0.724 0.320 10 114044277 missense variant A/G snv 0.15 0.17 17
rs1801253 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 34
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131