Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs74315401 0.683 0.320 20 4699525 missense variant C/T snv 32
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1805054 0.708 0.200 1 19666020 synonymous variant C/T snv 0.15; 8.0E-06 0.16 17
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169