Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562 0.463 0.714 6 26092913 missense variant G/A snp 3.3E-02 3.8E-02 175
rs6265 0.463 0.679 11 27658369 missense variant C/T snp 0.19 0.15 171
rs397507444 0.457 0.714 1 11794407 missense variant T/G snp 169
rs759834365 0.471 0.679 11 27658456 missense variant C/T snp 1.2E-05 157
rs1799945 0.475 0.679 6 26090951 missense variant C/G snp 0.11 9.9E-02 152
rs4986790 0.465 0.750 9 117713024 missense variant A/G,T snp 6.1E-02; 4.0E-06 6.7E-02 146
rs1799983 0.475 0.786 7 150999023 missense variant T/A,G snp 0.75 0.76 138
rs4986791 0.501 0.714 9 117713324 missense variant C/T snp 5.7E-02 5.1E-02 108
rs1801133 0.533 0.714 1 11796321 missense variant G/A snp 0.31 0.26 86
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
rs2476601 0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92 76
rs1805192 0.545 0.679 3 12379739 missense variant C/G snp 75
rs9939609
FTO
0.580 0.607 16 53786615 intron variant T/A snp 0.42 74
rs662 0.561 0.607 7 95308134 missense variant T/C snp 0.38 0.41 71
rs1800629
TNF
0.549 0.786 6 31575254 intergenic variant G/A snp 0.12 0.15 69
rs5443 0.570 0.571 12 6845711 synonymous variant C/T snp 0.36 0.43 65
rs1260326 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 63
rs7903146 0.596 0.536 10 112998590 intron variant C/G,T snp 0.26 59
rs1800795 0.580 0.607 7 22727026 intron variant C/G snp 0.68 58
rs738409 0.590 0.536 22 43928847 missense variant C/G snp 0.28 0.22 55
rs3184504 0.642 0.393 12 111446804 missense variant T/A,C,G snp 0.67 0.67 55
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
rs1229984 0.622 0.393 4 99318162 missense variant T/C,G snp 0.90 0.94 50