{{Rsnum
|rsid=1058808
|Gene=ERBB2
|Chromosome=17
|position=39727784
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=G
|GMAF=0.4908
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene_s=ERBB2
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 6.2 | 46.2 | 47.7
| HCB | 68.9 | 31.1 | 0.0
| JPT | 63.6 | 36.4 | 0.0
| YRI | 100.0 | 0.0 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 68.9 | 31.1 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}
{{PMID Auto
|PMID=19438491
|Title=The effects of obesity and HER-2 polymorphisms as risk factors for endometrial cancer in Korean women
}}

{{PharmGKB
|RSID=rs1058808
|Name_s=ERBB2: A1170P
|Gene_s=ERBB2, C17orf37
|Feature=
|Evidence=PubMed ID:15743501
|Annotation=Risk or phenotype-associated allele: none. Phenotype: Breast cancer risk. Study size: 2192 (1438 incident and 754 prevalent) cases and 2257 controls. Study population/ethnicity: British female breast cancer patients < 55 years of age (prevalent cases) recruited between 1 January 1991 and 30 June 1996, and < 70 years of age diagnosed from 1996 onwards (incident cases), and ethinic-matched European controls. Significance metric(s): p = 0.45 (non-significant). Type of association: GN; CO.
|Drugs=
|Drug Classes=
|Diseases=Breast Neoplasms
|Curation Level=Curated
|PharmGKB Accession ID=PA165290960
}}{{PMID|17267408|OA=1
}} Allelic imbalance in gene expression as a guide to cis-acting regulatory single nucleotide polymorphisms in cancer cells.

{{PMID|17598910|OA=1
}} Interactions among genes in the ErbB-Neuregulin signalling network are associated with increased susceptibility to schizophrenia.

{{PMID|19055823|OA=1
}} The genetic polymorphisms of HER-2 and the risk of lung cancer in a Korean population.

{{PMID|19336545|OA=1
}} Heritable variation of ERBB2 and breast cancer risk.{{GET Evidence
|gene=ERBB2
|aa_change=Pro1170Ala
|aa_change_short=P1170A
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1058808
|overall_frequency_n=5502
|overall_frequency_d=10756
|overall_frequency=0.511528
|n_genomes=38
|n_genomes_annotated=0
|n_haplomes=50
|n_articles=0
|n_articles_annotated=0
|pph2_score=0.983
|nblosum100=2
|autoscore=1
|webscore=N
}}
{{PMID Auto
|PMID=23200760
|Title=Pathway analysis of genome-wide association study on asthma
}}