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
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs1041981 0.667 0.520 6 31573007 missense variant C/A snv 0.35 0.38 25
rs1861494 0.716 0.400 12 68157629 intron variant C/T snv 0.75 15
rs1135216 0.807 0.200 6 32847198 missense variant T/C snv 0.17 0.18 6