PRNP, prion protein, 5621

N. diseases: 426; N. variants: 47
Disease: Neurodegenerative Disorders ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs74315401
rs74315401
Entrez Id: 5621
Gene Symbol: PRNP
PRNP
CUI: C0524851
Disease:
Neurodegenerative Disorders 		0.010 GeneticVariation BEFREE Due to the cerebellar ataxia in the early stage, GSS P102L is often misdiagnosed as other neurodegenerative disorders. 29509064 2018