DisGeNET - a database of gene-disease associations

Source: ALL

Disease: Parkinsonian Disorders ×

Variant: rs242557 ×

Results per page

Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _v

DPI _v

pLI

EI _vda

EL _gda

Score _vda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Variant

Gene

Disease

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

dbSNP:

rs242557

rs242557

MAPT

CUI:	C0242422
Disease:	Parkinsonian Disorders

Parkinsonian Disorders

0.010

GeneticVariation

BEFREE

The rs242557 polymorphism could act modulating the phenotypic expressivity of the H1 risk on these parkinsonisms.

2011