Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs2430561 0.590 0.760 12 68158742 intron variant T/A snv 0.36 50
rs1800471 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 48
rs1444669684 0.658 0.480 9 21994285 missense variant C/A;T snv 36
rs696 0.708 0.520 14 35401887 3 prime UTR variant C/T snv 0.45 22
rs1800777 0.724 0.280 16 56983407 missense variant G/A snv 3.7E-02 2.8E-02 17
rs2233406 0.732 0.440 14 35405593 upstream gene variant G/A snv 0.26 12
rs41507953 0.790 0.280 8 27500988 missense variant A/G snv 8.7E-02 0.13 10
rs121907892 0.807 0.240 11 64593747 stop gained G/A;C snv 2.8E-04 8
rs2276415 0.882 0.160 11 77590296 missense variant G/A snv 0.14 0.13 6
rs121907896 0.851 0.200 11 64591825 missense variant G/A snv 1.8E-04 8.4E-05 5
rs1451506414 0.882 0.200 11 64598561 synonymous variant G/A snv 4
rs782818582 0.882 0.160 9 133456116 stop gained C/T snv 1.2E-05 7.0E-06 3
rs753482595 0.925 0.200 4 9920389 missense variant T/C snv 8.0E-06 1.4E-05 3
rs10854554 0.925 0.080 22 19623159 regulatory region variant A/G snv 0.18 2
rs62341639 0.925 0.080 4 184238281 intergenic variant C/T snv 0.20 2
rs561633150 0.925 0.200 4 9980627 missense variant C/T snv 6.1E-04 9.1E-05 2
rs62341657 1.000 0.080 4 184238385 intergenic variant G/A snv 0.18 1
rs9617814 1.000 0.080 22 19622420 regulatory region variant A/G snv 0.22 1
rs12457893 1.000 0.080 18 63258928 intron variant A/C snv 0.39 1
rs8094315 1.000 0.080 18 63268814 intron variant A/G snv 0.17 1