MAPT, microtubule associated protein tau, 4137

N. diseases: 469; N. variants: 292
Disease: Supranuclear Palsy, Progressive, 1 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs63750959
rs63750959
Entrez Id: 4137
Gene Symbol: MAPT
MAPT
CUI: C4551863
Disease:
Supranuclear Palsy, Progressive, 1 		0.800 GeneticVariation UNIPROT
dbSNP: rs63750959
rs63750959
Entrez Id: 4137
Gene Symbol: MAPT
MAPT
CUI: C4551863
Disease:
Supranuclear Palsy, Progressive, 1 		T 0.800 CausalMutation CLINVAR
dbSNP: rs63751391
rs63751391
Entrez Id: 4137
Gene Symbol: MAPT
MAPT
CUI: C4551863
Disease:
Supranuclear Palsy, Progressive, 1 		0.800 GeneticVariation UNIPROT
dbSNP: rs63751391
rs63751391
Entrez Id: 4137
Gene Symbol: MAPT
MAPT
CUI: C4551863
Disease:
Supranuclear Palsy, Progressive, 1 		T 0.800 CausalMutation CLINVAR
dbSNP: rs63750424
rs63750424
Entrez Id: 4137
Gene Symbol: MAPT
MAPT
CUI: C4551863
Disease:
Supranuclear Palsy, Progressive, 1 		T 0.700 CausalMutation CLINVAR
dbSNP: rs63750425
rs63750425
Entrez Id: 4137
Gene Symbol: MAPT
MAPT
CUI: C4551863
Disease:
Supranuclear Palsy, Progressive, 1 		T 0.700 CausalMutation CLINVAR
dbSNP: rs63750756
rs63750756
Entrez Id: 4137
Gene Symbol: MAPT
MAPT
CUI: C4551863
Disease:
Supranuclear Palsy, Progressive, 1 		G 0.700 CausalMutation CLINVAR
dbSNP: rs63751273
rs63751273
Entrez Id: 4137
Gene Symbol: MAPT
MAPT
CUI: C4551863
Disease:
Supranuclear Palsy, Progressive, 1 		T 0.700 CausalMutation CLINVAR