Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 57
rs2279744 0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs243865 0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 78
rs28934578 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 47
rs79184941 0.617 0.600 10 121520163 missense variant G/A;C snv 5.6E-05; 4.0E-06 41
rs568408 0.649 0.600 3 159995680 3 prime UTR variant G/A snv 0.16 29
rs745738344
TNF
0.653 0.600 6 31576786 synonymous variant G/A snv 1.6E-05 1.4E-05 28
rs11556218 0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 27
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs17655 0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs121913499 0.605 0.520 2 208248389 missense variant G/A;C;T snv 51
rs5370 0.630 0.520 6 12296022 missense variant G/T snv 0.23 0.21 37
rs368087026 0.637 0.520 21 45530890 missense variant G/A snv 33
rs217727 0.641 0.480 11 1995678 non coding transcript exon variant G/A snv 0.20 34
rs28934573 0.667 0.480 17 7674241 missense variant G/A;C;T snv 4.0E-06 28
rs531564 0.672 0.480 8 9903189 non coding transcript exon variant G/C snv 0.14 27
rs1760944 0.672 0.480 14 20454990 non coding transcript exon variant T/C;G snv 26
rs764146326 0.662 0.480 17 7673779 missense variant C/A;G;T snv 4.0E-06 25
rs4778889 0.683 0.480 15 81296654 intron variant T/C snv 0.24 24
rs3217992 0.683 0.480 9 22003224 3 prime UTR variant C/T snv 0.32 22
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs747342068 0.695 0.440 17 7675218 missense variant T/C;G snv 4.0E-06 21
rs6218 0.732 0.440 12 102399855 3 prime UTR variant A/G snv 2.1E-02 13
rs3212986 0.620 0.400 19 45409478 stop gained C/A;G;T snv 0.29; 4.3E-06; 4.3E-06 42