Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3732379 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 38
rs767830104 0.752 0.280 2 136115399 missense variant C/G;T snv 4.0E-06; 8.0E-06 13
rs4244285 0.695 0.360 10 94781859 synonymous variant G/A;C snv 0.18 18
rs1187513719 0.851 0.200 10 94780595 missense variant A/G snv 4.0E-06 4
rs12095080 1.000 0.080 1 53911057 3 prime UTR variant A/G snv 0.12 2
rs225015 0.882 0.160 14 80201236 3 prime UTR variant G/A snv 0.37 5
rs1053874 0.851 0.240 16 3657746 missense variant G/A;T snv 0.36; 4.0E-06 7
rs4636297 0.724 0.360 9 136670698 intron variant A/G snv 0.67 0.65 14
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs1271572 0.708 0.400 14 64295199 intron variant A/C;T snv 16
rs5985 0.724 0.280 6 6318562 missense variant C/A;T snv 0.20; 2.4E-05 20
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs751377893
F5
0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 65
rs201058276
F7
0.776 0.240 13 113118731 missense variant G/A;C snv 4.8E-05; 4.0E-06 11
rs1183027238
F7
1.000 0.080 13 113118480 synonymous variant C/T snv 1
rs200478651
F7
1.000 0.080 13 113118414 splice region variant C/A;T snv 8.4E-06; 2.1E-05 1
rs4220
FGB
0.925 0.080 4 154570607 missense variant G/A snv 0.17 0.15 6
rs1445501474 1.000 0.080 18 22168521 intron variant G/T snv 1.4E-05 1
rs1416421760 1.000 0.080 18 22168362 non coding transcript exon variant C/A snv 1.4E-05 1
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
rs1201493098 1.000 0.080 17 4934295 missense variant A/G snv 4.0E-06 1.4E-05 1
rs1613662 0.851 0.120 19 55025227 missense variant G/A snv 0.85 0.83 8
rs1800730 0.649 0.480 6 26090957 missense variant A/T snv 1.0E-02 1.0E-02 32
rs41508050 0.882 0.080 14 61738090 missense variant C/T snv 3.8E-03 4.0E-03 4