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: rs121913400
rs121913400
CTNNB1
26 0.683 0.360 3 41224610 missense variant C/A;G;T snv 0.010 1.000 1 2001 2001
dbSNP: rs121913403
rs121913403
CTNNB1
23 0.683 0.240 3 41224622 missense variant C/A;G;T snv 0.010 1.000 1 2001 2001
dbSNP: rs28931589
rs28931589
CTNNB1
17 0.695 0.240 3 41224613 missense variant G/A;C;T snv 0.010 1.000 1 2001 2001
dbSNP: rs769708176
rs769708176
APC
2 1.000 0.080 5 112767243 missense variant C/G snv 1.2E-05 0.010 1.000 1 2001 2001