Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2844479 0.925 0.200 6 31605179 intergenic variant A/C snv 0.34 5
rs2231142 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs2023305 0.851 0.280 6 167111410 intron variant C/T snv 0.38 4
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 16
rs1256049 0.645 0.560 14 64257333 synonymous variant C/T snv 6.7E-02 6.3E-02 32
rs367732974
F7
0.790 0.360 13 113105788 5 prime UTR variant G/A snv 8.9E-05 2.8E-05 9
rs549591993
F7
0.776 0.400 13 113105794 5 prime UTR variant C/A snv 4.0E-04 2.8E-05 12
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs4684677 0.742 0.360 3 10286769 missense variant T/A snv 0.10 6.6E-02 13
rs281864525
HBB
0.851 0.280 11 5227097 5 prime UTR variant T/A;G snv 7.0E-06 4
rs63750953
HBB
0.790 0.400 11 5227097 5 prime UTR variant TT/- delins 7.0E-06 10
rs34166473
HBD
0.827 0.320 11 5234513 5 prime UTR variant A/G snv 7.0E-06 6
rs6314 0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02 23
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs2229113 0.763 0.360 11 117998955 missense variant A/G snv 0.74 0.74 10
rs3819024 0.701 0.560 6 52185988 upstream gene variant A/G snv 0.34 17
rs8193036 0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 21
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140