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
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
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
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs28933979
TTR
0.587 0.600 18 31592974 missense variant G/A;C snv 1.0E-04 70
rs4961 0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 27
rs1042636 0.672 0.360 3 122284922 missense variant A/G snv 0.15 9.0E-02 23
rs61747728 0.701 0.240 1 179557079 missense variant C/T snv 3.0E-02 2.8E-02 20
rs1044498 0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 15
rs11739136 0.827 0.200 5 170383792 missense variant C/T snv 9.9E-02 8.7E-02 10
rs4362
ACE
0.807 0.240 17 63496400 missense variant T/C;G snv 0.52; 1.2E-05 0.51 9
rs188942711 0.763 0.200 2 227253336 missense variant G/A;T snv 2.8E-05; 4.0E-06 9
rs4821480 0.807 0.160 22 36299201 intron variant G/T snv 0.78 9
rs7582694 0.763 0.400 2 191105394 intron variant C/G snv 0.77 9
rs3752462 0.827 0.160 22 36314138 splice region variant T/C snv 0.57 0.53 7
rs734553 0.851 0.240 4 9921380 intron variant G/A;T snv 7
rs151340626 0.827 0.200 X 50085987 missense variant C/T snv 5
rs867394500
ACE
0.851 0.080 17 63477301 missense variant G/T snv 4
rs151340624 0.851 0.120 X 50090846 stop gained C/T snv 4
rs104886303 0.851 0.200 X 108695409 missense variant T/G snv 4
rs3759126 0.882 0.080 12 49950079 upstream gene variant A/G snv 0.23 3
rs121908144 0.882 0.240 1 54999221 missense variant T/C snv 2.0E-05 3
rs4281481 0.882 0.080 11 22859013 intron variant C/G snv 0.36 3