Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs324420 0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs1051931 0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19
rs315952 0.763 0.400 2 113132727 missense variant T/A;C snv 4.0E-06; 0.31 10
rs1805018 0.827 0.200 6 46711566 missense variant A/G snv 6.8E-02 0.10 6
rs1320896171 0.882 0.120 17 2680294 missense variant C/T snv 7.0E-06 3