{{Rsnum
|rsid = 28933369
|Gene = ERBB2
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=A
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Chromosome=17
|position=39724744
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ERBB2,MIR4728
}}NOTE: the OMIM entry cited below refers to a somatic mutation, not a germline SNP

{{omim
|desc=GASTRIC CANCER, SOMATIC
|id=164870
|rsnum=28933369
|variant=0007
}}
{{ neighbor
| rsid = 28933370
| distance = 381
}}

{{ClinVar
|rsid=28933369
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=37880997
|CHROM=17
|dbSNPBuildID=126
|SSR=0
|SAO=3
|VP=0x050060000000000002110120
|GENEINFO=MIR4728:100616132; ERBB2:2064
|GENE_NAME=MIR4728; ERBB2
|GENE_ID=100616132; 2064
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.37880997G>A
|CLNORIGIN=1
|CLNSIG=255
|Tags=PM;OTHERKG;LSD;OM
|CLNACC=RCV000014893.1
|CLNDBN=Neoplasm of stomach
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=164870.0007
|Disease=Neoplasm of stomach
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0038356:613659:63443:126824007
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}