{{Rsnum
|rsid=121909334
|Chromosome=9
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=VCP
|position=35065255
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=VCP
}}{{omim
|id=601023
|rsnum=121909334
|variant=0006
}}{{ClinVar
|rsid=121909334
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=35065252
|CHROM=9
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=VCP:7415
|GENE_NAME=VCP
|GENE_ID=7415
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000009.11:g.35065252C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601023.0006
|CLNSIG=5
|CLNCUI=C1833662; C3151403
|CLNDBN=Inclusion body myopathy with early-onset paget disease and frontotemporal dementia; Amyotrophic lateral sclerosis 14, with or without frontotemporal dementia
|Disease=Inclusion body myopathy with early-onset paget disease and frontotemporal dementia; Amyotrophic lateral sclerosis 14
|CLNACC=RCV000008994.1; RCV000023064.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM; MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1476:C1833662:167320; C3151403:613954:803
}}