DisGeNET - a database of gene-disease associations

Summary of VDAs
Evidences for VDAs

rs2066842, NOD2

N. diseases: 15

Disease: Sporadic Parkinson disease ×

Source: BEFREE ×

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

Disease

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

Sporadic Parkinson disease

CUI:	C4511452
Disease:	Sporadic Parkinson disease

0.010

GeneticVariation

BEFREE

Our results suggested that the P268S variant in NOD2 might be a risk factor for susceptibility to sporadic Parkinson's disease in Chinese populations.

23651603

2013