DisGeNET - a database of gene-disease associations

Source: GWASCAT

Gene: LINC02210-CRHR1 ×

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:

rs2942168

LINC02210 ; LINC02210-CRHR1

CUI:	C0030567
Disease:	Parkinson Disease

Parkinson Disease

0.820

GeneticVariation

GWASCAT

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

21292315

2011

dbSNP:

rs393152

LINC02210 ; LINC02210-CRHR1

CUI:	C0030567
Disease:	Parkinson Disease

Parkinson Disease

0.810

GeneticVariation

GWASCAT

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

19915575

2009

dbSNP:

rs9303521

LINC02210-CRHR1

CUI:	C0005938
Disease:	Bone Density

Bone Density

0.800

GeneticVariation

GWASCAT

Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies.

19801982

2009

dbSNP:

rs112550936

LINC02210 ; LINC02210-CRHR1

CUI:	C0596887
Disease:	mathematical ability

mathematical ability

0.700

GeneticVariation

GWASCAT

Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals.

30038396

2018

dbSNP:

rs12150672

LINC02210-CRHR1

CUI:	C0014772
Disease:	Red Blood Cell Count measurement

Red Blood Cell Count measurement

0.700

GeneticVariation

GWASCAT

Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis.

28017375

2017

dbSNP:

rs12938031

LINC02210-CRHR1

CUI:	C0525045
Disease:	Mood Disorders

Mood Disorders

0.700

GeneticVariation

GWASCAT

Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways.

29942085

2018

dbSNP:

rs12938031

LINC02210-CRHR1

CUI:	C0003467
Disease:	Anxiety

Anxiety

0.700

GeneticVariation

GWASCAT

Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways.

29942085

2018

dbSNP:

rs12938031

LINC02210-CRHR1

CUI:	C1269683
Disease:	Major Depressive Disorder

Major Depressive Disorder

0.700

GeneticVariation

GWASCAT

Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways.

29942085

2018

dbSNP:

rs12938031

LINC02210-CRHR1

CUI:	C0021704
Disease:	Intelligence

Intelligence

0.700

GeneticVariation

GWASCAT

Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function.

29844566

2018

dbSNP:

rs143699161

LINC02210-CRHR1 ; LOC105371802

CUI:	C0596887
Disease:	mathematical ability

mathematical ability

0.700

GeneticVariation

GWASCAT

Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals.

30038396

2018

dbSNP:

rs143699161

LINC02210-CRHR1 ; LOC105371802

CUI:	C0021704
Disease:	Intelligence

Intelligence

0.700

GeneticVariation

GWASCAT

Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function.

29844566

2018

dbSNP:

rs1526123

LINC02210-CRHR1

CUI:	C0021704
Disease:	Intelligence

Intelligence

0.700

GeneticVariation

GWASCAT

Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function.

29844566

2018

dbSNP:

rs1724422

LINC02210-CRHR1

CUI:	C1269683
Disease:	Major Depressive Disorder

Major Depressive Disorder

0.700

GeneticVariation

GWASCAT

Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways.

29942085

2018

dbSNP:

rs1724422

LINC02210-CRHR1

CUI:	C0525045
Disease:	Mood Disorders

Mood Disorders

0.700

GeneticVariation

GWASCAT

Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways.

29942085

2018

dbSNP:

rs1724425

LINC02210-CRHR1

CUI:	C0021704
Disease:	Intelligence

Intelligence

0.700

GeneticVariation

GWASCAT

Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function.

29844566

2018

dbSNP:

rs17426174

LINC02210-CRHR1

CUI:	C0021704
Disease:	Intelligence

Intelligence

0.700

GeneticVariation

GWASCAT

A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence.

29326435

2019

dbSNP:

rs17563683

LINC02210-CRHR1 ; LOC107985028

CUI:	C0518015
Disease:	Hemoglobin measurement

Hemoglobin measurement

0.700

GeneticVariation

GWASCAT

The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.

27863252

2016

dbSNP:

rs17563683

LINC02210-CRHR1 ; LOC107985028

CUI:	C0018935
Disease:	Hematocrit procedure

Hematocrit procedure

0.700

GeneticVariation

GWASCAT

The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.

27863252

2016

dbSNP:

rs17688916

LINC02210-CRHR1

CUI:	C0424574
Disease:	Duration of sleep

Duration of sleep

0.700

GeneticVariation

GWASCAT

Genome-wide association study identifies genetic loci for self-reported habitual sleep duration supported by accelerometer-derived estimates.

30846698

2019

dbSNP:

rs1876829

CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1

CUI:	C0205682
Disease:	Waist-Hip Ratio

Waist-Hip Ratio

0.700

GeneticVariation

GWASCAT

Association of Genetic Variants Related to Gluteofemoral vs Abdominal Fat Distribution With Type 2 Diabetes, Coronary Disease, and Cardiovascular Risk Factors.

30575882

2018

dbSNP:

rs241036

LINC02210 ; LINC02210-CRHR1

CUI:	C1314691
Disease:	Age at menarche

Age at menarche

0.700

GeneticVariation

GWASCAT

Leveraging Polygenic Functional Enrichment to Improve GWAS Power.

30595370

2019

dbSNP:

rs34186148

LINC02210-CRHR1

CUI:	C1269683
Disease:	Major Depressive Disorder

Major Depressive Disorder

0.700

GeneticVariation

GWASCAT

Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways.

29942085

2018

dbSNP:

rs34186148

LINC02210-CRHR1

CUI:	C0525045
Disease:	Mood Disorders

Mood Disorders

0.700

GeneticVariation

GWASCAT

Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways.

29942085

2018

dbSNP:

rs35076622

LINC02210-CRHR1

CUI:	C0021704
Disease:	Intelligence

Intelligence

0.700

GeneticVariation

GWASCAT

Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways.

31374203

2019

dbSNP:

rs35076622

LINC02210-CRHR1

CUI:	C0036341
Disease:	Schizophrenia

Schizophrenia

0.700

GeneticVariation

GWASCAT

Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways.

31374203

2019