rs63750424, MAPT

N. diseases: 30
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Senile Plaques
CUI: C0333463
Disease: Senile Plaques
0.020 GeneticVariation BEFREE Frontotemporal dementia with parkinsonism linked to chromosome 17 with the MAPT R406W mutation presenting with a broad distribution of abundant senile plaques. 25377499 2015
Senile Plaques
CUI: C0333463
Disease: Senile Plaques
0.020 GeneticVariation BEFREE The first R406W</span> brain showed many NFT in affected regions with only a few diffuse amyloid plaques. 11193139 2000