{{Rsnum
|rsid=104894262
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=MEN1
|position=64807994
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MEN1
}}{{omim
|id=131100
|rsnum=104894262
|variant=0021
}}{{ClinVar
|rsid=104894262
|Reversed=1
|FwdREF=T
|FwdALT=A
|REF=A
|ALT=T
|RSPOS=64575466
|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.64575466A>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=613733.0021
|CLNSIG=5
|CLNCUI=C1840402
|CLNDBN=Hyperparathyroidism 1
|Disease=Hyperparathyroidism 1
|CLNACC=RCV000018177.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK3789:C1840402:145000
}}