rs63750424, MAPT

N. diseases: 30
Disease: Memory impairment ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Memory impairment
CUI: C0233794
Disease: Memory impairment
0.020 GeneticVariation BEFREE R406W patients often show a long course of disease with marked memory deficits. 29370822 2018
Memory impairment
CUI: C0233794
Disease: Memory impairment
0.020 GeneticVariation BEFREE Tau filament formation and associative memory deficit in aged mice expressing mutant (R406W) human tau. 12368474 2002