Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
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
rs1805192 0.545 0.679 3 12379739 missense variant C/G snp 75
rs1800629
TNF
0.549 0.786 6 31575254 intergenic variant G/A snp 0.12 0.15 69
rs7903146 0.596 0.536 10 112998590 intron variant C/G,T snp 0.26 59
rs5498 0.570 0.679 19 10285007 missense variant A/G snp 0.44 0.36 53
rs1800470 0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60 46
rs4994 0.605 0.536 8 37966280 missense variant A/G snp 0.11 9.0E-02 44
rs2070600 0.602 0.643 6 32183666 missense variant C/T snp 5.3E-02 4.4E-02 44
rs1800896 0.593 0.571 1 206773552 intergenic variant T/C snp 0.40 43
rs1501299 0.647 0.536 3 186853334 intron variant G/C,T snp 6.4E-05; 0.30 28
rs16139 0.657 0.500 7 24285260 missense variant T/A,C snp 4.0E-06; 3.0E-02 3.2E-02 27
rs1049353 0.657 0.464 6 88143916 synonymous variant C/T snp 0.21 0.20 26
rs699947 0.667 0.571 6 43768652 intergenic variant A/C,T snp 0.59 25
rs800292
CFH
0.679 0.464 1 196673103 missense variant G/A snp 0.32 0.39 22
rs745738344
TNF
0.679 0.500 6 31576786 stop gained G/A snp 1.6E-05 22
rs1799969 0.679 0.500 19 10284116 missense variant G/A snp 0.11 0.10 20
rs1799724 0.673 0.429 6 31574705 intergenic variant C/T snp 7.8E-02 20
rs3856806 0.715 0.357 3 12434058 synonymous variant C/T snp 0.13 0.13 18
rs361525
TNF
0.685 0.500 6 31575324 intergenic variant G/A snp 3.9E-02 17
rs80356814 0.724 0.321 1 156138697 synonymous variant C/T snp 8.0E-06 3.2E-05 16
rs8192678 0.734 0.286 4 23814039 missense variant C/T snp 0.31 0.26 16