{{Rsnum
|rsid=63750653
|Chromosome=3
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=CHMP2B
|position=87253421
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CHMP2B
}}{{omim
|id=609512
|rsnum=63750653
|variant=0002
}}

{{ClinVar
|rsid=63750653
|Reversed=0
|FwdREF=G
|FwdALT=T
|REF=G
|ALT=T
|RSPOS=87302571
|CHROM=3
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=CHMP2B:25978
|GENE_NAME=CHMP2B
|GENE_ID=25978
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.87302571G>T
|CLNSRC=GeneReviews; Neurodegenerative Brain Diseases Group; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK1199; ADM_379; 609512.0002
|CLNSIG=5
|CLNCUI=C1833296; C1833296
|CLNDBN=Frontotemporal Dementia, Chromosome 3-Linked; not provided
|Disease=Frontotemporal Dementia; not provided
|CLNACC=RCV000001720.1; RCV000084275.1
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1199:C1833296:600795:275864:282
}}

{{PMID Auto
|PMID=16041373
|Title=Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia.
}}

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