DisGeNET - a database of gene-disease associations

Source: ALL

Disease: Parkinson Disease ×

Variant: rs6656401 ×

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:

rs6656401

rs6656401

CR1

CUI:	C0030567
Disease:	Parkinson Disease

Parkinson Disease

0.010

GeneticVariation

BEFREE

The two other SNPs, rs6656401 from CR1, and rs3851179 from PICALM region were not associated with PD (p>0.05).

2011