Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 47
rs1799964 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 47
rs5743618 0.677 0.360 4 38797027 missense variant C/A snv 0.53 0.51 25
rs8177374 0.672 0.520 11 126292948 missense variant C/T snv 0.12 0.11 22
rs1800630 0.701 0.480 6 31574699 upstream gene variant C/A snv 0.14 17