Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042579 0.732 0.240 20 23048087 missense variant G/A;T snv 0.19 16
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1458766475 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs201058276
F7
0.776 0.240 13 113118731 missense variant G/A;C snv 4.8E-05; 4.0E-06 11
rs281865545 0.695 0.360 17 64377836 missense variant C/G;T snv 18
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4244285 0.695 0.360 10 94781859 synonymous variant G/A;C snv 0.18 18
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs5882 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
rs5985 0.724 0.280 6 6318562 missense variant C/A;T snv 0.20; 2.4E-05 20
rs63751001 0.790 0.240 16 16159555 missense variant C/T snv 2.8E-05 13
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs751377893
F5
0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 65
rs767830104 0.752 0.280 2 136115399 missense variant C/G;T snv 4.0E-06; 8.0E-06 13
rs770572030 0.827 0.160 18 49581427 missense variant T/A;C snv 4.0E-06; 4.0E-06 5
rs771676129 0.827 0.080 7 80671082 synonymous variant C/T snv 4.0E-06 7
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs999947969 0.827 0.080 7 80671145 synonymous variant C/T snv 7
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs72653706 0.695 0.480 16 16163078 stop gained G/A snv 1.4E-03 1.2E-03 32
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116