Gene: CTNNB1 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121913409
rs121913409
CTNNB1
0.820 GeneticVariation UNIPROT

dbSNP: rs121913409
rs121913409
CTNNB1
T 0.820 CausalMutation CLINVAR

dbSNP: rs121913407
rs121913407
CTNNB1
0.810 GeneticVariation UNIPROT

dbSNP: rs121913407
rs121913407
CTNNB1
C 0.810 CausalMutation CLINVAR

dbSNP: rs121913413
rs121913413
CTNNB1
0.810 GeneticVariation UNIPROT

dbSNP: rs121913228
rs121913228
CTNNB1
0.800 GeneticVariation UNIPROT

dbSNP: rs121913396
rs121913396
CTNNB1
0.800 GeneticVariation UNIPROT

dbSNP: rs121913399
rs121913399
CTNNB1
0.800 GeneticVariation UNIPROT

dbSNP: rs121913400
rs121913400
CTNNB1
0.800 GeneticVariation UNIPROT

dbSNP: rs121913403
rs121913403
CTNNB1
0.800 GeneticVariation UNIPROT

dbSNP: rs121913412
rs121913412
CTNNB1
0.800 GeneticVariation UNIPROT

dbSNP: rs28931588
rs28931588
CTNNB1
0.800 GeneticVariation UNIPROT

dbSNP: rs1413975856
rs1413975856
CTNNB1
0.700 GeneticVariation UNIPROT

dbSNP: rs1553631896
rs1553631896
CTNNB1
TA 0.700 CausalMutation CLINVAR

dbSNP: rs775104326
rs775104326
CTNNB1
T 0.700 CausalMutation CLINVAR

dbSNP: rs778624338
rs778624338
CTNNB1
A 0.700 CausalMutation CLINVAR

dbSNP: rs121913409
rs121913409
CTNNB1
0.820 GeneticVariation BEFREE GC-1 exerts a notable antitumoral effect on hMet-S45Y-β-catenin HCC by inactivating Met signaling. 28807594

2017
dbSNP: rs3864004
rs3864004
CTNNB1
0.020 GeneticVariation BEFREE Genotype GA (P = 0.001, OR = 0.567) and allele A (P = 0.002, OR = 0.652) of rs3864004, and genotype AG (P = 0.0004, OR = 0.495) and allele G (P = 0.001, OR = 0.596) of rs11564475 in the CTNNB1 gene were correlated with HCC compared with N-HCC patients. 28328801

2017
dbSNP: rs11564475
rs11564475
CTNNB1
0.010 GeneticVariation BEFREE Genotype GA (P = 0.001, OR = 0.567) and allele A (P = 0.002, OR = 0.652) of rs3864004, and genotype AG (P = 0.0004, OR = 0.495) and allele G (P = 0.001, OR = 0.596) of rs11564475 in the CTNNB1 gene were correlated with HCC compared with N-HCC patients. 28328801

2017
dbSNP: rs121913409
rs121913409
CTNNB1
G 0.820 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs121913409
rs121913409
CTNNB1
T 0.820 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs121913409
rs121913409
CTNNB1
A 0.820 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs121913407
rs121913407
CTNNB1
C 0.810 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs121913413
rs121913413
CTNNB1
A 0.810 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs121913413
rs121913413
CTNNB1
T 0.810 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016