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
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs2244608 0.882 0.160 12 120979185 intron variant A/G snv 0.29 9