DisGeNET - a database of gene-disease associations

Source: ALL

Disease: Coronary heart disease ×

Variant: rs11614913 ×

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:

rs11614913

HOXC6 ; MIR196A2

CUI:	C0010068
Disease:	Coronary heart disease

Coronary heart disease

0.030

GeneticVariation

BEFREE

Only rs11614913 was found to have significant associations with CHD.

31702616

2019

dbSNP:

rs11614913

HOXC6 ; MIR196A2

CUI:	C0010068
Disease:	Coronary heart disease

Coronary heart disease

0.030

GeneticVariation

BEFREE

miR-196a2 (rs11614913) polymorphism is associated with coronary artery disease, but not with in-stent coronary restenosis.

30560371

2019

dbSNP:

rs11614913

HOXC6 ; MIR196A2

CUI:	C0010068
Disease:	Coronary heart disease

Coronary heart disease

0.030

GeneticVariation

BEFREE

This is the first study to indicate that miR-196a2 rs11614913 plays a role in sporadic CHD susceptibility.

19514064

2009