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
rs61752717 0.583 0.840 16 3243407 missense variant T/A;C snv 2.8E-04 72
rs2066844 0.587 0.520 16 50712015 missense variant C/T snv 2.6E-02 2.9E-02 54
rs2066845 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 46
rs6908425 0.752 0.320 6 20728500 intron variant T/C snv 0.78 11
rs774359492 0.807 0.200 14 55008684 missense variant C/T snv 4.0E-06 7.0E-06 7