{{Rsnum
|rsid = 28931612
|Gene = MEN1
|geno1 = (A;A)
|geno2 = (A;G)
|geno3 = (G;G)
|Orientation=minus
|ReferenceAllele=G
|MissenseAllele=A
|Chromosome=11
|position=64810034
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MEN1
}}NOTE: the OMIM entry cited below refers to a somatic mutation, not a germline SNP

{{omim
|desc=PARATHYROID ADENOMA, SOMATIC
|id=131100
|rsnum=28931612
|variant=0013
}}

{{ClinVar
|rsid=28931612
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=64577506
|CHROM=11
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=MEN1:4221
|GENE_NAME=MEN1
|GENE_ID=4221
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.64577506C>T
|CLNORIGIN=1
|CLNSIG=255
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000018169.1
|CLNDBN=Parathyroid adenoma, somatic
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=613733.0013
|Disease=Parathyroid adenoma
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}