Gene: ERBB2 ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057519816
rs1057519816
ERBB2
T 0.710 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs1057519816
rs1057519816
ERBB2
A 0.710 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs1057519787
rs1057519787
ERBB2
A 0.700 GeneticVariation CLINVAR Functional analysis of receptor tyrosine kinase mutations in lung cancer identifies oncogenic extracellular domain mutations of ERBB2. 22908275

2012
dbSNP: rs1131692237
rs1131692237
ERBB2 ; MIR4728
G 0.700 CausalMutation CLINVAR

dbSNP: rs121913469
rs121913469
ERBB2
CC 0.700 CausalMutation CLINVAR

dbSNP: rs397516975
rs397516975
ERBB2 ; MIR4728
AGCATACGTGATG 0.700 CausalMutation CLINVAR

dbSNP: rs587776805
rs587776805
ERBB2 ; MIR4728
GTGTGGGCTC 0.700 CausalMutation CLINVAR