Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs63750756
rs63750756
Entrez Id: 4137
Gene Symbol: MAPT
MAPT
CUI: C4551863
Disease:
Supranuclear Palsy, Progressive, 1
G 0.700 CausalMutation CLINVAR