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
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs1800471 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 48
rs35068180 0.851 0.040 11 102845217 upstream gene variant A/-;AA delins 5