DisGeNET - a database of gene-disease associations

NBEA, neurobeachin, 26960

N. diseases: 5; N. variants: 9

Source: CURATED ×

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:

rs1777672

Entrez Id:	26960
Gene Symbol:	NBEA

NBEA

CUI:	C1836233
Disease:

AIDS, PROGRESSION TO

0.800

GeneticVariation

GWASCAT

Common genetic variation and the control of HIV-1 in humans.

20041166

2009

dbSNP:

rs1777672

Entrez Id:	26960
Gene Symbol:	NBEA

NBEA

CUI:	C1836230
Disease:

HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO

0.800

GeneticVariation

GWASCAT

Common genetic variation and the control of HIV-1 in humans.

20041166

2009

dbSNP:

rs1777672

Entrez Id:	26960
Gene Symbol:	NBEA

NBEA

CUI:	C1836232
Disease:

ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO

0.800

GeneticVariation

GWASCAT

Common genetic variation and the control of HIV-1 in humans.

20041166

2009

dbSNP:

rs1777672

Entrez Id:	26960
Gene Symbol:	NBEA

NBEA

CUI:	C1836231
Disease:

HIV-1, RESISTANCE TO

0.800

GeneticVariation

GWASDB

Common genetic variation and the control of HIV-1 in humans.

20041166

2009

dbSNP:

rs1777672

Entrez Id:	26960
Gene Symbol:	NBEA

NBEA

CUI:	C1836230
Disease:

HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO

0.800

GeneticVariation

GWASDB

Common genetic variation and the control of HIV-1 in humans.

20041166

2009

dbSNP:

rs1777672

Entrez Id:	26960
Gene Symbol:	NBEA

NBEA

CUI:	C1836233
Disease:

AIDS, PROGRESSION TO

0.800

GeneticVariation

GWASDB

Common genetic variation and the control of HIV-1 in humans.

20041166

2009

dbSNP:

rs1777672

Entrez Id:	26960
Gene Symbol:	NBEA

NBEA

CUI:	C1836232
Disease:

ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO

0.800

GeneticVariation

GWASDB

Common genetic variation and the control of HIV-1 in humans.

20041166

2009

dbSNP:

rs1777672

Entrez Id:	26960
Gene Symbol:	NBEA

NBEA

CUI:	C1836231
Disease:

HIV-1, RESISTANCE TO

0.800

GeneticVariation

GWASCAT

Common genetic variation and the control of HIV-1 in humans.

20041166

2009

dbSNP:

rs180940944

Entrez Id:	26960
Gene Symbol:	NBEA

NBEA

CUI:	C0699885
Disease:

Carcinoma of bladder

0.700

GeneticVariation

GWASCAT

Our study suggests that rs180940944 (NBEA) is associated with an increased NMIBC tumour size at the time of diagnosis.

31277774

2019

dbSNP:

rs9544156

Entrez Id:	26960
Gene Symbol:	NBEA

NBEA

CUI:	C0005890
Disease:

Body Height

0.700

GeneticVariation

GWASCAT

Leveraging Polygenic Functional Enrichment to Improve GWAS Power.

30595370

2019

dbSNP:

rs9544930

Entrez Id:	26960
Gene Symbol:	NBEA

NBEA

CUI:	C1305855
Disease:

Body mass index

0.700

GeneticVariation

GWASCAT

Leveraging Polygenic Functional Enrichment to Improve GWAS Power.

30595370

2019

dbSNP:

rs869312667

Entrez Id:	26960
Gene Symbol:	NBEA

NBEA

CUI:	C0026351
Disease:

Moderate intellectual disability

0.700

GeneticVariation

CLINVAR

NBEA: Developmental disease gene with early generalized epilepsy phenotypes.

30269351

2018

dbSNP:

rs869312667

Entrez Id:	26960
Gene Symbol:	NBEA

NBEA

CUI:	C0036572
Disease:

Seizures

0.700

GeneticVariation

CLINVAR

NBEA: Developmental disease gene with early generalized epilepsy phenotypes.

30269351

2018

dbSNP:

rs878853169

Entrez Id:	26960
Gene Symbol:	NBEA

NBEA

CUI:	C0036572
Disease:

Seizures

0.700

GeneticVariation

CLINVAR

NBEA: Developmental disease gene with early generalized epilepsy phenotypes.

30269351

2018

dbSNP:

rs878853169

Entrez Id:	26960
Gene Symbol:	NBEA

NBEA

CUI:	C0026351
Disease:

Moderate intellectual disability

0.700

GeneticVariation

CLINVAR

NBEA: Developmental disease gene with early generalized epilepsy phenotypes.

30269351

2018

dbSNP:

rs878853169

Entrez Id:	26960
Gene Symbol:	NBEA

NBEA

CUI:	C1857108
Disease:

Limitation of joint mobility

0.700

GeneticVariation

CLINVAR

NBEA: Developmental disease gene with early generalized epilepsy phenotypes.

30269351

2018

dbSNP:

rs878853169

Entrez Id:	26960
Gene Symbol:	NBEA

NBEA

CUI:	C0454644
Disease:

Delayed speech and language development

0.700

GeneticVariation

CLINVAR

NBEA: Developmental disease gene with early generalized epilepsy phenotypes.

30269351

2018

dbSNP:

rs9544444

Entrez Id:	26960
Gene Symbol:	NBEA

NBEA

CUI:	C0596887
Disease:

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:

rs9544444

Entrez Id:	26960
Gene Symbol:	NBEA

NBEA

CUI:	C0596887
Disease:

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:

rs9574095

Entrez Id:	26960
Gene Symbol:	NBEA

NBEA

CUI:	C0596887
Disease:

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:

rs9565436

Entrez Id:	26960
Gene Symbol:	NBEA

NBEA

CUI:	C0871470
Disease:

Systolic Pressure

0.700

GeneticVariation

GWASCAT

Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation.

27841878

2017