Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs2230926 0.662 0.440 6 137874929 missense variant T/C;G snv 4.0E-06; 5.4E-02 27
rs17757541 0.827 0.240 18 63212453 intron variant C/G;T snv 7
rs9610 0.882 0.240 11 118001371 3 prime UTR variant G/A;T snv 0.51 4
rs12566340 0.925 0.200 1 113877706 3 prime UTR variant C/A;T snv 3