Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444 0.457 0.714 1 11794407 missense variant T/G snp 169
rs1799983 0.475 0.786 7 150999023 missense variant T/A,G snp 0.75 0.76 138
rs1801133 0.533 0.714 1 11796321 missense variant G/A snp 0.31 0.26 86
rs1805087
MTR
0.538 0.679 1 236885200 missense variant A/G snp 0.20 0.21 75
rs662 0.561 0.607 7 95308134 missense variant T/C snp 0.38 0.41 71
rs5443 0.570 0.571 12 6845711 synonymous variant C/T snp 0.36 0.43 65
rs1801394 0.577 0.643 5 7870860 missense variant A/G snp 0.47 0.46 60
rs1061170
CFH
0.575 0.607 1 196690107 missense variant C/T snp 0.68 0.63 53
rs854560 0.599 0.500 7 95316772 missense variant A/C,G,N,T snp 0.29 0.29 51
rs964184 0.756 0.286 11 116778201 3 prime UTR variant G/C snp 0.83 41
rs1333049 0.715 0.286 9 22125504 intergenic variant G/C snp 0.41 30
rs1501299 0.647 0.536 3 186853334 intron variant G/C,T snp 6.4E-05; 0.30 28
rs1051266 0.647 0.500 21 45537880 missense variant T/C,G snp 0.55; 4.4E-06 0.51 28
rs579459 0.784 0.107 9 133278724 regulatory region variant C/T snp 0.20 23
rs11591147 0.699 0.143 1 55039974 missense variant G/A,T snp 1.2E-02 1.4E-02 21
rs3764261 0.769 0.179 16 56959412 intergenic variant C/A snp 0.31 19
rs599839 0.784 0.143 1 109279544 intergenic variant G/A,C snp 0.64; 6.4E-05 17
rs72653706 0.734 0.179 16 16163078 stop gained G/A snp 1.4E-03 1.3E-03 16
rs80356814 0.724 0.321 1 156138697 synonymous variant C/T snp 8.0E-06 3.2E-05 16
rs4291
ACE
0.784 0.107 17 63476833 regulatory region variant T/A,C snp 0.64 13
rs1122608 0.784 0.071 19 11052925 intron variant G/T snp 0.18 13
rs505151 0.769 0.214 1 55063514 missense variant G/A snp 0.95 0.89 12
rs749437638 0.769 0.179 22 19968597 C/T snp 2.4E-05 3.2E-05 11
rs4746 0.769 0.250 6 38682852 missense variant T/A,G snp 0.36 0.38 10
rs387906592 0.878 0.107 10 88941309 missense variant C/T snp 6