Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1004467 0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14 13
rs1024610 0.882 0.200 17 34253212 upstream gene variant T/A snv 0.85 3
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs10401969 0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs1041981 0.667 0.520 6 31573007 missense variant C/A snv 0.35 0.38 25
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
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1049353 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs1050450 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 43
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
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
rs10738610 0.882 0.120 9 22123767 intron variant A/C;T snv 5
rs10740055 0.790 0.240 10 61958720 intron variant C/A snv 0.49 7
rs10741657 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs10754558 0.695 0.480 1 247448734 3 prime UTR variant G/C;T snv 20
rs10757274 0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs10757283 0.827 0.120 9 22134173 intergenic variant C/A;T snv 0.45 6
rs10761600 0.925 0.120 10 61997361 intron variant A/G;T snv 3
rs10767664 0.752 0.400 11 27704439 intron variant T/A snv 0.83 16
rs1081161 0.925 0.120 22 12200388 intergenic variant G/A snv 2