Gene: CTNNB1 ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs28931588
rs28931588
CTNNB1
T 0.820 CausalMutation CLINVAR

dbSNP: rs121913403
rs121913403
CTNNB1
G 0.810 CausalMutation CLINVAR

dbSNP: rs121913403
rs121913403
CTNNB1
T 0.810 CausalMutation CLINVAR

dbSNP: rs121913396
rs121913396
CTNNB1
G 0.800 CausalMutation CLINVAR

dbSNP: rs121913400
rs121913400
CTNNB1
T 0.800 CausalMutation CLINVAR

dbSNP: rs121913400
rs121913400
CTNNB1
A 0.800 CausalMutation CLINVAR

dbSNP: rs121913413
rs121913413
CTNNB1
T 0.800 CausalMutation CLINVAR

dbSNP: rs28931589
rs28931589
CTNNB1
A 0.800 CausalMutation CLINVAR

dbSNP: rs121913399
rs121913399
CTNNB1
A 0.700 GeneticVariation CLINVAR Prospective enterprise-level molecular genotyping of a cohort of cancer patients. 25157968

2014
dbSNP: rs121913399
rs121913399
CTNNB1
C 0.700 GeneticVariation CLINVAR Prospective enterprise-level molecular genotyping of a cohort of cancer patients. 25157968

2014
dbSNP: rs775104326
rs775104326
CTNNB1
T 0.700 CausalMutation CLINVAR