Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs11066280 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27
rs4072037 0.732 0.240 1 155192276 splice acceptor variant C/A;T snv 0.59 22
rs11066015 0.925 0.120 12 111730205 intron variant G/A snv 5.9E-03 5