Gene entry
VCP
valosin containing protein
- Chromosome
- 9
- Cytoband
- 9p13.3
- Variants (rsID)
- 5
VCP is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 9 (region 9p13.3). Its official name is “valosin containing protein”. The reference table lists 5 variants (rsID) for this gene.
Clinically classified variants
4 reference-table entries with clinical significance.
- rs10972300Benignsingle nucleotide variantInclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1|Frontotemporal dementia and/or amyotrophic lateral sclerosis 6|Charcot-Marie-Tooth disease type 2Y
- rs45537335Conflicting interpretationssingle nucleotide variantInclusion Body Myopathy, Dominant|Fanconi anemia|Amyotrophic Lateral Sclerosis, Dominant|Fanconi anemia complementation group G
- rs121909330Pathogenicsingle nucleotide variantInclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia|Frontotemporal dementia and/or amyotrophic lateral sclerosis 6|Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
- rs121909335Pathogenicsingle nucleotide variantInclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia|Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.