DisGeNET - a database of gene-disease associations

Parkinson Disease, C0030567

Variant: rs417968 ×

Source: ALL

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

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

dbSNP:

rs417968

LINC02210 ; LINC02210-CRHR1

0.700

GeneticVariation

GWASDB

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

24842889

2014

dbSNP:

rs417968

LINC02210 ; LINC02210-CRHR1

0.700

GeneticVariation

GWASDB

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

22438815

2012

dbSNP:

rs417968

LINC02210 ; LINC02210-CRHR1

0.700

GeneticVariation

GWASDB

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

21738487

2011

dbSNP:

rs417968

LINC02210 ; LINC02210-CRHR1

0.700

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

dbSNP:

rs417968

LINC02210 ; LINC02210-CRHR1

0.700

GeneticVariation

GWASDB

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

19915575

2009