DisGeNET - a database of gene-disease associations

LRRC37A2, leucine rich repeat containing 37 member A2, 474170

N. diseases: 7; N. variants: 70

Disease: Parkinson Disease ×

Variant: rs199515 ×

Source: ALL

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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:

rs199515

Entrez Id:	7473;474170
Gene Symbol:	WNT3;LRRC37A2

WNT3;LRRC37A2

CUI:	C0030567
Disease:

Parkinson Disease

0.800

GeneticVariation

GWASDB

Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2.

22451204

2012