{{Rsnum
|rsid=121909333
|Chromosome=9
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=VCP
|position=35065363
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Status=Merged
|Merged=121909329
|Gene_s=VCP
}}{{omim
|id=601023
|rsnum=121909333
|variant=0005
}}{{ClinVar
|rsid=121909333
|Reversed=1
|FwdREF=G
|FwdALT=C
|REF=C
|ALT=G
|RSPOS=35065360
|CHROM=9
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=050260000a15000002110100
|GENEINFO=VCP:7415
|GENE_NAME=VCP
|GENE_ID=7415
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000009.11:g.35065360C>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601023.0005
|CLNSIG=5
|CLNCUI=C1833662
|CLNDBN=Inclusion body myopathy with early-onset paget disease and front
|Disease=Inclusion body myopathy with early-onset paget disease and front
|CLNACC=SCV000029207.1
|Tags=RV;PM;S3D;NSM;REF;OTH;ASP;OTHERKG;LSD;OM
}}