rs772092699, EPHB2

N. diseases: 3
Disease: HER2 gene amplification ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
HER2 gene amplification
CUI: C1512127
Disease: HER2 gene amplification
0.010 GeneticVariation BEFREE Drug resistance becomes inevitable due to the emergence of the second-site EGFR T790M mutation within exon 20, MET and HER2 amplification, small cell histologic transformation and rare secondary BRAF mutations. 31132355 2019