MAPT, microtubule associated protein tau, 4137

N. diseases: 469; N. variants: 292
Disease: Parkinson Disease ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs17563965
rs17563965
Entrez Id: 4137
Gene Symbol: MAPT
MAPT
CUI: C0030567
Disease:
Parkinson Disease 		0.010 GeneticVariation BEFREE Two-SNP haplotypes inferred from rs17563965 and rs17649641 also showed association with PD (P = 0.018) and age at onset (P = 0.026). 21063069 2010