Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249