Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121913409
rs121913409
CTNNB1
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		0.820 GeneticVariation BEFREE Oncogenic potential of N-terminal deletion and S45Y mutant β-catenin in promoting hepatocellular carcinoma development in mice. 30419856

2018
dbSNP: rs121913409
rs121913409
CTNNB1
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		0.820 GeneticVariation BEFREE GC-1 exerts a notable antitumoral effect on hMet-S45Y-β-catenin HCC by inactivating Met signaling. 28807594

2017
dbSNP: rs121913409
rs121913409
CTNNB1
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		G 0.820 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs121913409
rs121913409
CTNNB1
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		T 0.820 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs121913409
rs121913409
CTNNB1
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		A 0.820 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs121913409
rs121913409
CTNNB1
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		0.820 GeneticVariation UNIPROT

dbSNP: rs121913409
rs121913409
CTNNB1
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		T 0.820 CausalMutation CLINVAR

dbSNP: rs121913407
rs121913407
CTNNB1
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		C 0.810 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs121913407
rs121913407
CTNNB1
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		0.810 GeneticVariation BEFREE Only three HCC cases (5.6%) were found mutated at residues (G34E, S45P, P44S, T41I) important for phosphorylation and ubiquitination of beta-catenin protein. 25536643

2015
dbSNP: rs121913407
rs121913407
CTNNB1
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		0.810 GeneticVariation UNIPROT

dbSNP: rs121913407
rs121913407
CTNNB1
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		C 0.810 CausalMutation CLINVAR

dbSNP: rs121913413
rs121913413
CTNNB1
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		A 0.810 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs121913413
rs121913413
CTNNB1
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		T 0.810 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs121913413
rs121913413
CTNNB1
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		0.810 GeneticVariation BEFREE Only three HCC cases (5.6%) were found mutated at residues (G34E, S45P, P44S, T41I) important for phosphorylation and ubiquitination of beta-catenin protein. 25536643

2015
dbSNP: rs121913413
rs121913413
CTNNB1
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		0.810 GeneticVariation UNIPROT

dbSNP: rs121913228
rs121913228
CTNNB1
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		C 0.800 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs121913228
rs121913228
CTNNB1
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		G 0.800 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs121913228
rs121913228
CTNNB1
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		0.800 GeneticVariation UNIPROT

dbSNP: rs121913396
rs121913396
CTNNB1
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		C 0.800 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs121913396
rs121913396
CTNNB1
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		T 0.800 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs121913396
rs121913396
CTNNB1
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		G 0.800 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs121913396
rs121913396
CTNNB1
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		0.800 GeneticVariation UNIPROT

dbSNP: rs121913399
rs121913399
CTNNB1
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		C 0.800 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs121913399
rs121913399
CTNNB1
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		0.800 GeneticVariation UNIPROT

dbSNP: rs121913400
rs121913400
CTNNB1
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		A 0.800 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016