DisGeNET - a database of gene-disease associations

Source: GWASDB

Disease: Coronary heart disease ×

Variant: rs10757278 ×

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:

rs10757278

CDKN2B-AS1

CUI:	C0010068
Disease:	Coronary heart disease

Coronary heart disease

0.800

GeneticVariation

GWASDB

A genome-wide association study of a coronary artery disease risk variant.

23364394

2013

dbSNP:

rs10757278

CDKN2B-AS1

CUI:	C0010068
Disease:	Coronary heart disease

Coronary heart disease

0.800

GeneticVariation

GWASDB

Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease.

22751097

2012

dbSNP:

rs10757278

CDKN2B-AS1

CUI:	C0010068
Disease:	Coronary heart disease

Coronary heart disease

0.800

GeneticVariation

GWASDB

Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project.

21347282

2011