Gene: PRNP ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs747019990
rs747019990
PRNP
0.010 GeneticVariation BEFREE PRNP P39L Variant is a Rare Cause of Frontotemporal Dementia in Italian Population. 26757195

2016
dbSNP: rs74315401
rs74315401
PRNP
0.010 GeneticVariation BEFREE Atypical frontotemporal dementia as a new clinical phenotype of Gerstmann-Straussler-Scheinker disease with the PrP-P102L mutation. Description of a previously unreported Italian family. 19030774

2008