MAPT, microtubule associated protein tau, 4137

N. diseases: 469; N. variants: 292
Disease: Primary Progressive Nonfluent Aphasia ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs63750869
rs63750869
Entrez Id: 4137
Gene Symbol: MAPT
MAPT
CUI: C0751706
Disease:
Primary Progressive Nonfluent Aphasia 		0.020 GeneticVariation BEFREE The V363I mutation of the microtubule-associated protein tau gene has previously been associated with a case of primary progressive nonfluent aphasia with variable penetrance. 21343707 2011
dbSNP: rs63750869
rs63750869
Entrez Id: 4137
Gene Symbol: MAPT
MAPT
CUI: C0751706
Disease:
Primary Progressive Nonfluent Aphasia 		0.020 GeneticVariation BEFREE Progressive nonfluent aphasia associated with a new mutation V363I in tau gene. 17712160 2007