EPHB2, EPH receptor B2, 2048

N. diseases: 649; N. variants: 19
Disease: HER2 gene amplification ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs772092699
rs772092699
Entrez Id: 2048
Gene Symbol: EPHB2
EPHB2
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