RS1554668168 VCP
Upload your DNA to see your genotype for this variant.
Associated Conditions
Inborn genetic diseases
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Inborn genetic diseases
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Other Variants in VCP