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
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs1883832 0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs11556218 0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 27