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
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 62
rs1799964 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 46
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 45
rs745738344
TNF
0.653 0.600 6 31576786 synonymous variant G/A snv 1.6E-05 1.4E-05 28
rs1800630 0.701 0.480 6 31574699 upstream gene variant C/A snv 0.14 17
rs1800610
TNF
0.807 0.320 6 31576050 intron variant G/A snv 8.4E-02 6