Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs116843064 0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02 16