{{Rsnum
|rsid=63751126
|Chromosome=3
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=CHMP2B
|position=87253798
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CHMP2B
}}{{omim
|id=609512
|rsnum=63751126
|variant=0003
}}{{ClinVar
|rsid=63751126
|Reversed=0
|FwdREF=A
|FwdALT=C
|REF=A
|ALT=C
|RSPOS=87302948
|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.87302948A>C
|CLNSRC=GeneReviews; Neurodegenerative Brain Diseases Group; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK1199; ADM_385; 609512.0003
|CLNSIG=5
|CLNCUI=C1833296
|CLNDBN=Amyotrophic lateral sclerosis 17; Frontotemporal Dementia, Chromosome 3-Linked; not provided
|Disease=Amyotrophic lateral sclerosis 17; Frontotemporal Dementia; not provided
|CLNACC=RCV000001721.2; RCV000020696.1; RCV000084279.1
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet; GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=C1836076:614696:803; NBK1199:C1833296:600795:275864:282
}}{{PMID Auto
|PMID=16807408
|Title=ALS phenotypes with mutations in CHMP2B (charged multivesicular body protein 2B).
}}