DisGeNET - a database of gene-disease associations

Coronary heart disease, C0010068

Variant: rs3782889 ×

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

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

dbSNP:

rs3782889

rs3782889

MYL2

C

0.800

GeneticVariation

GWASCAT

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

2013

dbSNP:

rs3782889

rs3782889

MYL2

C

0.800

GeneticVariation

GWASDB

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

2013