rs74315413, PRNP

N. diseases: 8
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Dementia
CUI: C0497327
Disease: Dementia
0.010 GeneticVariation BEFREE PRNP H187R mutation associated with neuropsychiatric disorders in childhood and dementia. 15824374 2005