Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs77150043 0.724 0.240 16 50270338 intron variant C/T snv 0.17 14
rs78534766 0.827 0.080 16 50301163 missense variant C/A snv 4.3E-03 3.6E-03 7