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: rs121913399
rs121913399
CTNNB1
13 0.724 0.200 3 41224612 missense variant G/A;C snv 0.710 1.000 2 2009 2014