Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35
rs3218716 0.716 0.280 14 23425316 missense variant C/A;G;T snv 4.0E-06; 2.4E-05 17
rs121908987 0.742 0.200 7 151576412 missense variant C/A;G;T snv 4.0E-06 12
rs587782958 0.790 0.120 11 47333552 splice region variant C/T snv 1.7E-05 10
rs121913628 0.763 0.160 14 23424059 missense variant C/G;T snv 10
rs3218713 0.763 0.160 14 23431468 missense variant C/A;T snv 10
rs104894369 0.807 0.080 12 110914287 missense variant C/A;T snv 10
rs193922680 0.790 0.080 15 34793398 missense variant C/T snv 4.0E-06 7.0E-06 9
rs267606908 0.763 0.160 14 23424112 missense variant T/C snv 4.0E-06 7.0E-06 9
rs3218714 0.763 0.160 14 23429279 missense variant G/A;C snv 9
rs371898076 0.763 0.160 14 23426833 missense variant C/T snv 8.0E-06 4.9E-05 9
rs397516127 0.763 0.160 14 23426834 missense variant G/A;C snv 9
rs397516171 0.763 0.160 14 23424041 missense variant C/G;T snv 9
rs397516264 0.763 0.160 14 23431602 missense variant C/T snv 4.0E-06 9
rs104894503 0.776 0.160 15 63060899 missense variant G/A snv 1.6E-05 2.8E-05 9
rs104894845 0.807 0.160 X 101401752 missense variant C/G;T snv 5.5E-04 8
rs121913627 0.851 0.080 14 23427657 missense variant C/A;G;T snv 4.0E-06 8
rs104894724 0.790 0.120 19 55154146 missense variant G/A;C snv 4.0E-06 8
rs397516354 0.790 0.120 19 55154094 missense variant C/A;G;T snv 4.0E-05 8
rs121909374 0.790 0.120 11 47342578 stop gained C/A;G snv 1.3E-05 7
rs121913630 0.851 0.080 14 23425814 missense variant G/A;C snv 1.2E-05 7
rs267607490
DES
0.925 0.160 2 219425734 missense variant C/T snv 6
rs587782951 0.807 0.080 20 44160305 missense variant G/T snv 6