Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs5370 0.630 0.520 6 12296022 missense variant G/T snv 0.23 0.21 37
rs1800206 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
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
rs7799039 0.649 0.560 7 128238730 upstream gene variant G/A;C snv 33
rs5219 0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 25
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
rs1800437 0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 13
rs5068 0.776 0.160 1 11845917 3 prime UTR variant A/G;T snv 13
rs10423928 0.807 0.200 19 45679046 intron variant T/A snv 0.19 12
rs1320702652 0.752 0.160 15 43824536 missense variant G/A snv 4.0E-06 11
rs10189761 0.882 0.120 2 646364 intergenic variant T/A snv 0.82 4