{{Rsnum
|rsid=63750818
|Chromosome=3
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CHMP2B
|position=87240749
|Gene_s=CHMP2B
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=63750818
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=87289899
|CHROM=3
|dbSNPBuildID=137
|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.87289899A>G
|CLNSRC=GeneReviews; Neurodegenerative Brain Diseases Group; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK1199; ADM_384; 609512.0005
|CLNSIG=5
|CLNCUI=C1833296
|CLNDBN=Frontotemporal Dementia, Chromosome 3-Linked; Amyotrophic lateral sclerosis 17; not provided
|Disease=Frontotemporal Dementia; Amyotrophic lateral sclerosis 17; not provided
|CLNACC=RCV000020697.3; RCV000029146.2; RCV000084271.1
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet; MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1199:C1833296:600795:275864:282; C1836076:614696:803
}}

{{PMID Auto
|PMID=16431024
|Title=CHMP2B mutations are not a common cause of frontotemporal lobar degeneration.
}}

{{PMID Auto
|PMID=16807408
|Title=ALS phenotypes with mutations in CHMP2B (charged multivesicular body protein 2B).
}}

{{PMID Auto
|PMID=16941655
|Title=CHMP2B mutations are not a cause of dementia in Dutch patients with familial and sporadic frontotemporal dementia.
}}

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