rs63750424, MAPT

N. diseases: 30
Disease: Amnesia ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Amnesia
CUI: C0002622
Disease: Amnesia
0.010 GeneticVariation BEFREE MAPT p.R406W carriers present clinically with progressive memory loss and neuropathologically with neuronal and glial tauopathy. 30546007 2018