Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121913355
rs121913355
BRAF
0.720 GeneticVariation BEFREE Acquired BRAF G469A Mutation as a Resistance Mechanism to First-Line Osimertinib Treatment in NSCLC Cell Lines Harboring an EGFR Exon 19 Deletion. 31502118

2019
dbSNP: rs121913355
rs121913355
BRAF
0.720 GeneticVariation BEFREE A molecular characterization of NSCLC and HCC lesions was performed, revealing a BRAF exon 11 mutation (G469V) only in NSCLC. 27388325

2016
dbSNP: rs121913355
rs121913355
BRAF
A 0.720 CausalMutation CLINVAR Mutations of the BRAF gene in human cancer. 12068308

2002
dbSNP: rs121913355
rs121913355
BRAF
G 0.720 CausalMutation CLINVAR Mutations of the BRAF gene in human cancer. 12068308

2002