Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10137082 0.925 0.080 14 23370824 upstream gene variant C/T snv 0.23 2
rs1020608562 0.807 0.160 3 46373738 missense variant T/C snv 4.0E-06 9
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs1033182 0.882 0.160 6 151873899 intron variant G/A snv 0.26 3
rs10404257 0.925 0.080 19 38645846 upstream gene variant G/A snv 0.50 2
rs1042636 0.672 0.360 3 122284922 missense variant A/G snv 0.15 9.0E-02 23
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1044498 0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 15
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs104894833 0.776 0.280 X 101403984 missense variant C/G snv 1.2E-04 1.9E-05 11
rs1049255 0.776 0.320 16 88643329 3 prime UTR variant C/T snv 0.49 0.48 9
rs1057518923 0.925 0.200 16 2115395 frameshift variant -/C delins 3
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs10808565 0.925 0.080 8 127995166 non coding transcript exon variant C/T snv 0.31 2
rs10887800 0.790 0.280 10 88316086 intron variant A/G;T snv 11
rs10951982 0.851 0.160 7 6382925 intron variant G/A;T snv 5
rs11089781 0.925 0.080 22 36160720 stop gained G/A snv 1.6E-02 6.5E-02 2
rs11089788 0.851 0.120 22 36355056 intron variant C/A snv 0.46 5
rs112417755 1.000 0.080 10 8073738 splice acceptor variant G/C;T snv 1
rs115489112 0.925 0.080 19 35830918 missense variant G/A snv 4.3E-04 1.6E-03 2
rs11571317 0.882 0.160 2 203867285 upstream gene variant C/T snv 5.2E-02 3
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs1162592300
ALB
0.925 0.080 4 73412045 missense variant G/A snv 3
rs11643718 0.807 0.240 16 56899607 missense variant G/A snv 0.11 8.4E-02 10
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102