Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057519837
rs1057519837
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.710 GeneticVariation BEFREE Of interest, mutation analyses revealed the presence of an identical point mutation, c.98C>G, in exon 3 of β-catenin (CTNNB1) in both tumors. 21881488

2011