Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 17
rs12369009 12 111581995 intron variant G/T snv 0.63 1
rs695871 1.000 0.080 12 111599196 missense variant G/C snv 0.77 0.61 1