DisGeNET - a database of gene-disease associations

Acute Coronary Syndrome, C0948089

Variant: rs41507953 ×

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:

rs41507953

rs41507953

EPHX2

0.010

GeneticVariation

BEFREE

Association between the EPHX2 p.Lys55Arg polymorphism and prognosis following an acute coronary syndrome.

2018