DisGeNET - a database of gene-disease associations

Coronary heart disease, C0010068

Variant: rs1044925 ×

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:

rs1044925

rs1044925

SOAT1

0.010

GeneticVariation

BEFREE

Association between single nucleotide polymorphism rs1044925 and the risk of coronary artery disease and ischemic stroke.

2014