Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1010 0.807 0.120 2 85581859 3 prime UTR variant T/C;G snv 7
rs10118757 0.827 0.120 9 21853340 intron variant A/G snv 0.26 7
rs10159239 0.882 0.040 1 247443750 intron variant G/A snv 0.57 3
rs1035071612 0.763 0.240 19 11113361 missense variant C/A;T snv 4.0E-06 9
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
rs1042579 0.732 0.240 20 23048087 missense variant G/A;T snv 0.19 16
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
rs1044925 0.827 0.120 1 179354603 3 prime UTR variant C/A;G snv 6
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
rs1048990 0.790 0.280 14 35292469 5 prime UTR variant C/G;T snv 0.19; 4.0E-06 8
rs1049255 0.776 0.320 16 88643329 3 prime UTR variant C/T snv 0.49 0.48 9
rs1049353 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs1049673 0.807 0.160 7 80677034 3 prime UTR variant C/G;T snv 7
rs1050450 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 43
rs10509681 0.807 0.160 10 95038992 missense variant T/C snv 8.3E-02 8.0E-02 8
rs1051338 0.807 0.120 10 89247603 missense variant T/G snv 0.32 0.26 7
rs1051339 0.882 0.040 10 89247582 missense variant C/T snv 9.5E-02 0.13 3
rs1051931 0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1058930 0.882 0.040 10 95058362 missense variant G/A;C snv 1.0E-04; 3.7E-02 4
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