Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs884164 0.925 0.040 19 4521613 upstream gene variant A/G;T snv 2
rs872129 0.925 0.080 1 203200263 intergenic variant A/G snv 0.19 2
rs7944926 0.807 0.200 11 71454579 intron variant A/G snv 0.54 7
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs77375493 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs753152 0.882 0.160 17 42761487 intron variant T/G snv 0.12 6
rs752596535 0.752 0.200 19 11105407 stop gained C/A;G;T snv 1.6E-05 14
rs751141 0.732 0.400 8 27516348 missense variant G/A snv 0.12 0.10 16
rs750249283 0.925 0.080 21 42296256 missense variant C/G;T snv 4.0E-06; 8.0E-06 2
rs745738344
TNF
0.653 0.600 6 31576786 synonymous variant G/A snv 1.6E-05 1.4E-05 28
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs72653706 0.695 0.480 16 16163078 stop gained G/A snv 1.4E-03 1.2E-03 32
rs7043199 1.000 0.040 9 2621145 intron variant T/A snv 0.18 2
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs6993770 0.925 0.080 8 105569300 intron variant A/T snv 0.31 9
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs6921438 0.776 0.360 6 43957870 intergenic variant G/A;C snv 10
rs6834314 0.807 0.160 4 87292656 intergenic variant A/G snv 0.24 10
rs6749704 0.827 0.240 2 227813126 intron variant T/C snv 0.24 5
rs6742078 0.807 0.240 2 233763993 intron variant G/T snv 0.36 13
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs6025
F5
0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 43
rs5882 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
rs5880 0.827 0.040 16 56981179 missense variant G/C snv 5.2E-02 3.7E-02 10