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
rs1045642 0.520 0.714 7 87509329 synonymous variant A/G,T snp 0.50 0.56 108
rs2910164 0.525 0.750 5 160485411 mature miRNA variant C/G snp 0.71; 4.1E-06 0.71 82
rs4880 0.536 0.643 6 159692840 missense variant A/G snp 0.48 0.47 81
rs1801282 0.543 0.679 3 12351626 missense variant C/G snp 0.11 1.0E-01 77
rs1805087
MTR
0.538 0.679 1 236885200 missense variant A/G snp 0.20 0.21 75
rs1805192 0.545 0.679 3 12379739 missense variant C/G snp 75
rs5443 0.570 0.571 12 6845711 synonymous variant C/T snp 0.36 0.43 65
rs1061170
CFH
0.575 0.607 1 196690107 missense variant C/T snp 0.68 0.63 53
rs11614913 0.585 0.607 12 53991815 mature miRNA variant C/T snp 0.39 0.35 49
rs1800470 0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60 46
rs2070600 0.602 0.643 6 32183666 missense variant C/T snp 5.3E-02 4.4E-02 44
rs3746444 0.596 0.500 20 34990448 mature miRNA variant A/G snp 0.20 0.18 40
rs1042713 0.622 0.571 5 148826877 missense variant G/A snp 0.42 0.43 38
rs1800469 0.622 0.571 19 41354391 intron variant A/G snp 0.70 32
rs6280 0.652 0.357 3 114171968 missense variant C/T snp 0.63 0.56 31
rs3732378 0.667 0.500 3 39265671 missense variant G/A snp 0.14 0.12 28
rs2292832 0.657 0.429 2 240456086 non coding transcript exon variant T/A,C snp 0.59 0.69 23
rs4961 0.685 0.250 4 2904980 missense variant G/A,T snp 1.2E-05; 0.20 0.17 22
rs5370 0.715 0.250 6 12296022 missense variant G/T snp 0.23 0.21 17
rs3743930 0.715 0.464 16 3254626 missense variant C/G,T snp 7.1E-02 2.6E-02 17
rs3732379 0.715 0.357 3 39265765 missense variant C/T snp 0.22 0.22 15
rs17817449
FTO
0.769 0.321 16 53779455 intron variant T/A,G snp 0.39 14
rs121913059
CFH
0.744 0.214 1 196747245 missense variant C/T snp 1.4E-04 1.6E-04 11