Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs2070744 0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs2430561 0.590 0.760 12 68158742 intron variant T/A snv 0.36 50
rs1946518 0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs2227306 0.677 0.680 4 73741338 intron variant C/T snv 0.31 21
rs1861494 0.716 0.400 12 68157629 intron variant C/T snv 0.75 15
rs9264942 0.763 0.400 6 31306603 intron variant T/C snv 0.34 15
rs843720 0.752 0.280 2 54283523 intron variant T/G snv 0.52 10
rs1520220 0.807 0.280 12 102402744 intron variant G/C;T snv 0.76 9
rs6677604
CFH
0.827 0.200 1 196717788 intron variant G/A snv 0.23 7
rs3218896 0.807 0.160 2 102015190 intron variant T/C;G snv 6
rs10490571 0.827 0.320 2 102100877 intron variant C/T snv 0.29 5
rs11089788 0.851 0.120 22 36355056 intron variant C/A snv 0.46 5
rs2412971 0.882 0.320 22 30098382 intron variant G/A snv 0.55 5
rs719250 0.827 0.200 2 102007256 intron variant C/T snv 0.11 5
rs12615793 0.851 0.280 2 54248777 intron variant G/A;T snv 4
rs4849121 0.925 0.160 2 110842129 intron variant G/A snv 0.44 3
rs11102930 0.925 0.160 1 115338434 intron variant G/A snv 0.54 2
rs11150619 0.925 0.160 16 31365528 intron variant T/C snv 0.29 2
rs3759334 0.925 0.120 12 6382842 intron variant G/A snv 0.26 2
rs7190997 1.000 0.120 16 31356857 intron variant T/C snv 0.52 2
rs9314614 1.000 0.120 8 6840209 intron variant C/G snv 0.61 2
rs1008898 1.000 0.120 7 7233928 intron variant G/A;T snv 1