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
rs324011 0.742 0.360 12 57108399 intron variant C/T snv 0.32 12
rs6967330 0.827 0.120 7 106018005 missense variant G/A snv 0.19 0.21 8
rs2664538 0.827 0.200 20 46011586 missense variant A/G snv 6