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
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
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
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
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
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs953038635 0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 51
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs3743930 0.611 0.720 16 3254626 missense variant C/G;T snv 7.1E-02 43
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs17577 0.649 0.520 20 46014472 missense variant G/A;C snv 0.16 31
rs281865545 0.695 0.360 17 64377836 missense variant C/G;T snv 18
rs10865710 0.763 0.360 3 12311699 intron variant C/G snv 0.25 13
rs174566 0.925 0.160 11 61824890 intron variant A/G snv 0.34 8