Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs79105258 12 111280427 intron variant C/A;T snv 23
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 21
rs4835265 4 145900258 intron variant C/A snv 0.15 5