Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs4335411
rs4335411
PGBD2
3 1.000 1 248897507 regulatory region variant G/A snv 0.82 0.700 1.000 1 2018 2018