Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs10757274 0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs10911021 0.807 0.160 1 182112825 intron variant C/T snv 0.36 11
rs11066001 0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 15
rs12785878 0.677 0.520 11 71456403 intron variant G/A;T snv 25
rs12979860 0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs174547 0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs1800588 0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 16
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs184003 0.724 0.400 6 32182519 intron variant C/A snv 0.12 0.12 15
rs2383207 0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs4717806 0.776 0.200 7 73702147 intron variant T/A;C snv 9
rs780093 0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs10757283 0.827 0.120 9 22134173 intergenic variant C/A;T snv 0.45 6
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1050450 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 43
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs1063856
VWF
0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 14
rs1129844 0.752 0.320 17 34285875 missense variant G/A;C;T snv 0.16; 1.2E-05 13