Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121913413
rs121913413
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
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
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
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.810 GeneticVariation UNIPROT