Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs72653706 0.695 0.480 16 16163078 stop gained G/A snv 1.4E-03 1.2E-03 32
rs7493 0.677 0.440 7 95405463 missense variant G/C snv 0.27 0.27 24
rs2383207 0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
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
rs281865545 0.695 0.360 17 64377836 missense variant C/G;T snv 18
rs4244285 0.695 0.360 10 94781859 synonymous variant G/A;C snv 0.18 18
rs1042579 0.732 0.240 20 23048087 missense variant G/A;T snv 0.19 16
rs1122608 0.763 0.120 19 11052925 intron variant G/T snv 0.18 16
rs63751001 0.790 0.240 16 16159555 missense variant C/T snv 2.8E-05 13
rs767830104 0.752 0.280 2 136115399 missense variant C/G;T snv 4.0E-06; 8.0E-06 13
rs201058276
F7
0.776 0.240 13 113118731 missense variant G/A;C snv 4.8E-05; 4.0E-06 11
rs771676129 0.827 0.080 7 80671082 synonymous variant C/T snv 4.0E-06 7
rs999947969 0.827 0.080 7 80671145 synonymous variant C/T snv 7
rs770572030 0.827 0.160 18 49581427 missense variant T/A;C snv 4.0E-06; 4.0E-06 5