MAPT, microtubule associated protein tau, 4137

N. diseases: 469; N. variants: 292
Disease: Child Development Disorders, Pervasive ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs141455452
rs141455452
Entrez Id: 4137
Gene Symbol: MAPT
MAPT
CUI: C0008074
Disease:
Child Development Disorders, Pervasive 		T 0.700 GeneticVariation GWASCAT Identification of common genetic risk variants for autism spectrum disorder. 30804558 2019