Source: BEFREE ×
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: rs28931588
rs28931588
CTNNB1
5 0.701 0.200 3 41224606 missense variant G/A;C;T snv 0.820 1.000 2 1999 2009
dbSNP: rs121913403
rs121913403
CTNNB1
10 0.683 0.240 3 41224622 missense variant C/A;G;T snv 0.810 1.000 1 1999 2017