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
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs1222213359 0.574 0.720 6 43770966 missense variant G/A snv 62
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 58
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs11209026 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs6025
F5
0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 43
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs10889677 0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs5370 0.630 0.520 6 12296022 missense variant G/T snv 0.23 0.21 37
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35
rs1799889 0.649 0.600 7 101126430 upstream gene variant A/G snv 31
rs11549467 0.653 0.400 14 61740857 missense variant G/A snv 8.9E-03 7.0E-03 30
rs2890565 0.732 0.440 1 7849677 missense variant C/T snv 8.7E-02 5.6E-02 15
rs2536512 0.752 0.280 4 24799693 missense variant G/A;T snv 0.55 14
rs1177506410
AGT
0.776 0.240 1 230706148 missense variant G/C snv 4.0E-06 7.0E-06 12