DisGeNET - a database of gene-disease associations

Source: GWASDB

Disease: Parkinson Disease ×

Gene: LINC02210-CRHR1 ×

Results per page

Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _g

DPI _g

pLI

EI _gda

EL _gda

Score _gda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Gene

Disease

Score _gda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

Entrez Id:	104909134
Gene Symbol:	LINC02210-CRHR1

LINC02210-CRHR1

CUI:	C0030567
Disease:	Parkinson Disease

Parkinson Disease

0.100

GeneticVariation

GWASDB

Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes.

24842889

2014

Entrez Id:	104909134
Gene Symbol:	LINC02210-CRHR1

LINC02210-CRHR1

CUI:	C0030567
Disease:	Parkinson Disease

Parkinson Disease

0.100

GeneticVariation

GWASDB

Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.

22438815

2012

Entrez Id:	104909134
Gene Symbol:	LINC02210-CRHR1

LINC02210-CRHR1

CUI:	C0030567
Disease:	Parkinson Disease

Parkinson Disease

0.100

GeneticVariation

GWASDB

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

22451204

2012

Entrez Id:	104909134
Gene Symbol:	LINC02210-CRHR1

LINC02210-CRHR1

CUI:	C0030567
Disease:	Parkinson Disease

Parkinson Disease

0.100

GeneticVariation

GWASDB

Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease.

21738487

2011

Entrez Id:	104909134
Gene Symbol:	LINC02210-CRHR1

LINC02210-CRHR1

CUI:	C0030567
Disease:	Parkinson Disease

Parkinson Disease

0.100

GeneticVariation

GWASDB

Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21.

21044948

2011

Entrez Id:	104909134
Gene Symbol:	LINC02210-CRHR1

LINC02210-CRHR1

CUI:	C0030567
Disease:	Parkinson Disease

Parkinson Disease

0.100

GeneticVariation

GWASDB

Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies.

21292315

2011

Entrez Id:	104909134
Gene Symbol:	LINC02210-CRHR1

LINC02210-CRHR1

CUI:	C0030567
Disease:	Parkinson Disease

Parkinson Disease

0.100

GeneticVariation

GWASDB

Genome-wide association study reveals genetic risk underlying Parkinson's disease.

19915575

2009