DisGeNET - a database of gene-disease associations

SNHG32, small nucleolar RNA host gene 32, 50854

N. diseases: 12; N. variants: 4

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:

rs9368699

Entrez Id:	26801;50854
Gene Symbol:	SNORD48;SNHG32

SNORD48;SNHG32

CUI:	C1836233
Disease:

AIDS, PROGRESSION TO

0.800

GeneticVariation

GWASDB

The major genetic determinants of HIV-1 control affect HLA class I peptide presentation.

21051598

2010

dbSNP:

rs9368699

Entrez Id:	26801;50854
Gene Symbol:	SNORD48;SNHG32

SNORD48;SNHG32

CUI:	C1836230
Disease:

HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO

0.800

GeneticVariation

GWASDB

The major genetic determinants of HIV-1 control affect HLA class I peptide presentation.

21051598

2010

dbSNP:

rs9368699

Entrez Id:	26801;50854
Gene Symbol:	SNORD48;SNHG32

SNORD48;SNHG32

CUI:	C1836232
Disease:

ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO

0.800

GeneticVariation

GWASDB

The major genetic determinants of HIV-1 control affect HLA class I peptide presentation.

21051598

2010

dbSNP:

rs9368699

Entrez Id:	26801;50854
Gene Symbol:	SNORD48;SNHG32

SNORD48;SNHG32

CUI:	C1836231
Disease:

HIV-1, RESISTANCE TO

0.800

GeneticVariation

GWASDB

The major genetic determinants of HIV-1 control affect HLA class I peptide presentation.

21051598

2010

dbSNP:

rs9368699

Entrez Id:	26801;50854
Gene Symbol:	SNORD48;SNHG32

SNORD48;SNHG32

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:

rs9368699

Entrez Id:	26801;50854
Gene Symbol:	SNORD48;SNHG32

SNORD48;SNHG32

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:

rs9368699

Entrez Id:	26801;50854
Gene Symbol:	SNORD48;SNHG32

SNORD48;SNHG32

CUI:	C1836233
Disease:

AIDS, PROGRESSION TO

0.800

GeneticVariation

GWASCAT

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

20041166

2009

dbSNP:

rs9368699

Entrez Id:	26801;50854
Gene Symbol:	SNORD48;SNHG32

SNORD48;SNHG32

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:

rs9368699

Entrez Id:	26801;50854
Gene Symbol:	SNORD48;SNHG32

SNORD48;SNHG32

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:

rs9368699

Entrez Id:	26801;50854
Gene Symbol:	SNORD48;SNHG32

SNORD48;SNHG32

CUI:	C1836233
Disease:

AIDS, PROGRESSION TO

0.800

GeneticVariation

GWASDB

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

20041166

2009

dbSNP:

rs9368699

Entrez Id:	26801;50854
Gene Symbol:	SNORD48;SNHG32

SNORD48;SNHG32

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:

rs9368699

Entrez Id:	26801;50854
Gene Symbol:	SNORD48;SNHG32

SNORD48;SNHG32

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:

rs115487693

Entrez Id:	50854
Gene Symbol:	SNHG32

SNHG32

CUI:	C0032181
Disease:

Platelet Count measurement

0.700

GeneticVariation

GWASCAT

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

27863252

2016

dbSNP:

rs17201248

Entrez Id:	26797;26801;50854
Gene Symbol:	SNORD52;SNORD48;SNHG32

SNORD52;SNORD48;SNHG32

CUI:	C0018213
Disease:

Graves Disease

0.700

GeneticVariation

GWASCAT

Genetic determinants of antithyroid drug-induced agranulocytosis by human leukocyte antigen genotyping and genome-wide association study.

26151496

2015

dbSNP:

rs17201248

Entrez Id:	26797;26801;50854
Gene Symbol:	SNORD52;SNORD48;SNHG32

SNORD52;SNORD48;SNHG32

CUI:	C0272178
Disease:

Drug-induced neutropenia

0.700

GeneticVariation

GWASCAT

Genetic determinants of antithyroid drug-induced agranulocytosis by human leukocyte antigen genotyping and genome-wide association study.

26151496

2015

dbSNP:

rs9368699

Entrez Id:	26801;50854
Gene Symbol:	SNORD48;SNHG32

SNORD48;SNHG32

CUI:	C0011615
Disease:

Dermatitis, Atopic

0.700

GeneticVariation

GWASDB

A genome-wide association study of atopic dermatitis identifies loci with overlapping effects on asthma and psoriasis.

23886662

2013

dbSNP:

rs3130679

Entrez Id:	50854
Gene Symbol:	SNHG32

SNHG32

CUI:	C0003873
Disease:

Rheumatoid Arthritis

0.700

GeneticVariation

GWASDB

A genome-wide association study suggests contrasting associations in ACPA-positive versus ACPA-negative rheumatoid arthritis.

21156761

2011

dbSNP:

rs9368699

Entrez Id:	26801;50854
Gene Symbol:	SNORD48;SNHG32

SNORD48;SNHG32

CUI:	C0001175
Disease:

Acquired Immunodeficiency Syndrome

0.700

GeneticVariation

GWASDB

Genomewide association study of an AIDS-nonprogression cohort emphasizes the role played by HLA genes (ANRS Genomewide Association Study 02).

19115949

2009

dbSNP:

rs9368699

Entrez Id:	26801;50854
Gene Symbol:	SNORD48;SNHG32

SNORD48;SNHG32

CUI:	C0011854
Disease:

Diabetes Mellitus, Insulin-Dependent

0.700

GeneticVariation

GWASDB

A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene.

17632545

2007

dbSNP:

rs9368699

Entrez Id:	26801;50854
Gene Symbol:	SNORD48;SNHG32

SNORD48;SNHG32

CUI:	C0033860
Disease:

Psoriasis

0.010

GeneticVariation

BEFREE

We found a strong association of two psoriasis MHC variants, rs9264942 and rs3021366, with both HIV-1 controller status and viral load, and identified another Class III MHC variant rs9368699 to be strongly associated with viral load.

27810495

2017