{{Rsnum
|rsid=104894259
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=MEN1
|position=64805078
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MAP4K2,MEN1
}}{{omim
|id=131100
|rsnum=104894259
|variant=0010
}}{{ClinVar
|rsid=104894259
|Reversed=1
|FwdREF=T
|FwdALT=A,C
|REF=A
|ALT=G,T
|RSPOS=64572550
|CHROM=11
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=MAP4K2:5871; MEN1:4221
|GENE_NAME=MAP4K2; MEN1
|GENE_ID=5871; 4221
|WGT=0
|VC=SNV
|CLNALLE=2
|CLNHGVS=NC_000011.9:g.64572550A>T
|CLNORIGIN=1
|CLNSRCID=
613733.0010
|CLNSIG=5
|CLNCUI=
|CLNACC=
RCV000018166.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDBN=Multiple endocrine neoplasia, type 1
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1538:C0025267:131100:652:30664006
|CLNSRC=OMIM Allelic Variant
|Disease=Multiple endocrine neoplasia
}}