Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
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
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs5186 0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs5219 0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 25
rs911119 0.807 0.120 20 23632100 non coding transcript exon variant C/G;T snv 9