Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1744297
ASPG
14 104102135 intron variant T/C snv 0.86 12
rs9549153
LINC00598
13 40293411 intron variant G/A snv 0.15 2
rs992037
PRKN
6 161580404 intron variant T/C snv 0.71 2