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
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
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs1800471 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 48
rs17319721 0.925 0.080 4 76447694 intron variant G/A snv 0.34 5
rs7456421 0.882 0.120 7 139715976 synonymous variant G/C snv 0.27 0.37 4