Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs63750424
rs63750424
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

dbSNP: rs63750424
rs63750424
0.020 GeneticVariation BEFREE The first R406W</span> brain showed many NFT in affected regions with only a few diffuse amyloid plaques. 11193139

2000