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
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs34637584 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs61752717 0.583 0.840 16 3243407 missense variant T/A;C snv 2.8E-04 72
rs751377893
F5
0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 65
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs2236225 0.614 0.640 14 64442127 missense variant G/A snv 0.44 0.38 52
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs5361 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 47
rs1458766475 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs3732379 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 38
rs5882 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
rs1801253 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 34
rs1800730 0.649 0.480 6 26090957 missense variant A/T snv 1.0E-02 1.0E-02 32
rs121917864 0.645 0.520 4 153704936 missense variant C/T snv 8.8E-05 9.8E-05 31
rs7493 0.677 0.440 7 95405463 missense variant G/C snv 0.27 0.27 24
rs5985 0.724 0.280 6 6318562 missense variant C/A;T snv 0.20; 2.4E-05 20
rs1051931 0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19
rs11053646 0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13 18
rs1805123 0.724 0.280 7 150948446 missense variant T/A;C;G snv 1.3E-05; 0.18; 8.4E-06 18