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
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs601338 0.742 0.280 19 48703417 stop gained G/A snv 0.38 0.45 19
rs4251961 0.763 0.200 2 113116890 intron variant T/C snv 0.29 10
rs2294021 0.776 0.280 X 49249149 intron variant T/A;C snv 0.52 8