Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs1878406 0.807 0.200 4 147472512 intergenic variant C/A;G;T snv 7
rs3869109 0.851 0.160 6 31216419 intergenic variant A/G;T snv 5
rs501120 0.763 0.240 10 44258419 downstream gene variant T/C snv 0.24 10
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
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
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs805297 0.851 0.280 6 31654829 intron variant C/A snv 0.23 6
rs17757541 0.827 0.240 18 63212453 intron variant C/G;T snv 7
rs2043211 0.653 0.480 19 48234449 missense variant A/T snv 0.33 0.29 29
rs1883832 0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs1129055 0.724 0.400 3 122119472 missense variant G/A snv 0.30 0.25 15
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs3217992 0.683 0.480 9 22003224 3 prime UTR variant C/T snv 0.32 22
rs2072633 0.807 0.320 6 31951801 3 prime UTR variant A/G snv 0.59 6
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs4950928 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 16
rs644045 0.851 0.240 6 31916180 intron variant A/G snv 0.72 4
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101