DisGeNET - a database of gene-disease associations

LRRC37A2, leucine rich repeat containing 37 member A2, 474170

N. diseases: 7; N. variants: 70

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

Disease

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

dbSNP:

rs141554661

Entrez Id:	9570;474170
Gene Symbol:	GOSR2;LRRC37A2

GOSR2;LRRC37A2

CUI:	C0751778
Disease:

Myoclonic Epilepsies, Progressive

0.700

GeneticVariation

CLINVAR

A mutation in the Golgi Qb-SNARE gene GOSR2 causes progressive myoclonus epilepsy with early ataxia.

21549339

2011

dbSNP:

rs1568177307

Entrez Id:	9570;474170
Gene Symbol:	GOSR2;LRRC37A2

GOSR2;LRRC37A2

CUI:	C0751778
Disease:

Myoclonic Epilepsies, Progressive

0.700

GeneticVariation

CLINVAR

A mutation in the Golgi Qb-SNARE gene GOSR2 causes progressive myoclonus epilepsy with early ataxia.

21549339

2011

dbSNP:

rs169201

Entrez Id:	4905;474170
Gene Symbol:	NSF;LRRC37A2

NSF;LRRC37A2

CUI:	C0030567
Disease:

Parkinson Disease

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:

rs17608766

Entrez Id:	9570;474170
Gene Symbol:	GOSR2;LRRC37A2

GOSR2;LRRC37A2

CUI:	C0428886
Disease:

Mean blood pressure

0.700

GeneticVariation

GWASCAT

Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.

21909110

2011

dbSNP:

rs17608766

Entrez Id:	9570;474170
Gene Symbol:	GOSR2;LRRC37A2

GOSR2;LRRC37A2

CUI:	C1306620
Disease:

Systolic blood pressure measurement

0.700

GeneticVariation

GWASDB

Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.

21909115

2011

dbSNP:

rs17608766

Entrez Id:	9570;474170
Gene Symbol:	GOSR2;LRRC37A2

GOSR2;LRRC37A2

CUI:	C0871470
Disease:

Systolic Pressure

0.700

GeneticVariation

GWASCAT

Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.

21909115

2011

dbSNP:

rs17608766

Entrez Id:	9570;474170
Gene Symbol:	GOSR2;LRRC37A2

GOSR2;LRRC37A2

CUI:	C0005823
Disease:

Blood Pressure

0.700

GeneticVariation

GWASDB

Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.

21909110

2011

dbSNP:

rs2074404

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

WNT3;LRRC37A2

CUI:	C0030567
Disease:

Parkinson Disease

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:

rs7224296

Entrez Id:	4905;474170
Gene Symbol:	NSF;LRRC37A2

NSF;LRRC37A2

CUI:	C0030567
Disease:

Parkinson Disease

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:

rs8069437

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

WNT3;LRRC37A2

CUI:	C0005823
Disease:

Blood Pressure

0.700

GeneticVariation

GWASDB

Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.

21909110

2011

dbSNP:

rs183211

Entrez Id:	4905;474170
Gene Symbol:	NSF;LRRC37A2

NSF;LRRC37A2

CUI:	C0030567
Disease:

Parkinson Disease

0.800

GeneticVariation

GWASDB

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

22438815

2012

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

dbSNP:

rs199515

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

WNT3;LRRC37A2

CUI:	C0030567
Disease:

Parkinson Disease

0.800

GeneticVariation

GWASCAT

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

22451204

2012

dbSNP:

rs199533

Entrez Id:	4905;474170
Gene Symbol:	NSF;LRRC37A2

NSF;LRRC37A2

CUI:	C0030567
Disease:

Parkinson Disease

0.800

GeneticVariation

GWASDB

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

22438815

2012

dbSNP:

rs142167

Entrez Id:	4905;474170
Gene Symbol:	NSF;LRRC37A2

NSF;LRRC37A2

CUI:	C4528257
Disease:

Corpuscular Hemoglobin Concentration Mean

0.700

GeneticVariation

GWASDB

Seventy-five genetic loci influencing the human red blood cell.

23222517

2012

dbSNP:

rs169201

Entrez Id:	4905;474170
Gene Symbol:	NSF;LRRC37A2

NSF;LRRC37A2

CUI:	C0030567
Disease:

Parkinson Disease

0.700

GeneticVariation

GWASDB

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

22438815

2012

dbSNP:

rs183211

Entrez Id:	4905;474170
Gene Symbol:	NSF;LRRC37A2

NSF;LRRC37A2

CUI:	C4528257
Disease:

Corpuscular Hemoglobin Concentration Mean

0.700

GeneticVariation

GWASDB

Seventy-five genetic loci influencing the human red blood cell.

23222517

2012

dbSNP:

rs199436

Entrez Id:	4905;474170
Gene Symbol:	NSF;LRRC37A2

NSF;LRRC37A2

CUI:	C4528257
Disease:

Corpuscular Hemoglobin Concentration Mean

0.700

GeneticVariation

GWASDB

Seventy-five genetic loci influencing the human red blood cell.

23222517

2012

dbSNP:

rs199438

Entrez Id:	4905;474170
Gene Symbol:	NSF;LRRC37A2

NSF;LRRC37A2

CUI:	C4528257
Disease:

Corpuscular Hemoglobin Concentration Mean

0.700

GeneticVariation

GWASDB

Seventy-five genetic loci influencing the human red blood cell.

23222517

2012

dbSNP:

rs199439

Entrez Id:	4905;474170
Gene Symbol:	NSF;LRRC37A2

NSF;LRRC37A2

CUI:	C4528257
Disease:

Corpuscular Hemoglobin Concentration Mean

0.700

GeneticVariation

GWASDB

Seventy-five genetic loci influencing the human red blood cell.

23222517

2012

dbSNP:

rs199442

Entrez Id:	4905;474170
Gene Symbol:	NSF;LRRC37A2

NSF;LRRC37A2

CUI:	C4528257
Disease:

Corpuscular Hemoglobin Concentration Mean

0.700

GeneticVariation

GWASDB

Seventy-five genetic loci influencing the human red blood cell.

23222517

2012

dbSNP:

rs199445

Entrez Id:	4905;474170
Gene Symbol:	NSF;LRRC37A2

NSF;LRRC37A2

CUI:	C4528257
Disease:

Corpuscular Hemoglobin Concentration Mean

0.700

GeneticVariation

GWASDB

Seventy-five genetic loci influencing the human red blood cell.

23222517

2012

dbSNP:

rs199448

Entrez Id:	4905;474170
Gene Symbol:	NSF;LRRC37A2

NSF;LRRC37A2

CUI:	C0008312
Disease:

Primary biliary cirrhosis

0.700

GeneticVariation

GWASDB

Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis.

22961000

2012

dbSNP:

rs199448

Entrez Id:	4905;474170
Gene Symbol:	NSF;LRRC37A2

NSF;LRRC37A2

CUI:	C4528257
Disease:

Corpuscular Hemoglobin Concentration Mean

0.700

GeneticVariation

GWASDB

Seventy-five genetic loci influencing the human red blood cell.

23222517

2012

dbSNP:

rs199452

Entrez Id:	4905;474170
Gene Symbol:	NSF;LRRC37A2

NSF;LRRC37A2

CUI:	C4528257
Disease:

Corpuscular Hemoglobin Concentration Mean

0.700

GeneticVariation

GWASDB

Seventy-five genetic loci influencing the human red blood cell.

23222517

2012