Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs387907272 0.572 0.520 3 38141150 stop lost T/C snv 5.2E-05 7.0E-06 73
rs121912438 0.605 0.520 21 31667299 missense variant G/A;C;T snv 1.2E-05; 8.0E-06 58
rs17655 0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs2230926 0.662 0.440 6 137874929 missense variant T/C;G snv 4.0E-06; 5.4E-02 27
rs9808753 0.701 0.400 21 33415005 missense variant A/G snv 0.20 0.18 17
rs1057520009 0.790 0.200 2 61492337 missense variant C/T snv 4.4E-06 14
rs11886868 0.752 0.280 2 60493111 intron variant C/T snv 0.65 12
rs1800477 0.763 0.480 18 63318540 missense variant C/T snv 1.8E-02 4.9E-03 12
rs4671393 0.790 0.400 2 60493816 intron variant A/C;G snv 11
rs104893626 0.827 0.280 2 136114915 stop gained G/C snv 11
rs1494555 0.790 0.120 5 35871088 missense variant G/A snv 0.64 0.72 8
rs17757541 0.827 0.240 18 63212453 intron variant C/G;T snv 7
rs2509049 0.827 0.160 11 119095811 upstream gene variant C/A;T snv 6
rs773862672 0.882 0.280 1 11247922 missense variant G/A;C snv 1.2E-05 6
rs78768932
PXN
0.882 0.080 12 120222977 missense variant C/G;T snv 5.4E-03 5.4E-03 6
rs2069812
IL5
0.851 0.240 5 132544224 intron variant A/G snv 0.54 5