DisGeNET - a database of gene-disease associations

Coronary Artery Disease, C1956346

Variant: rs3748067 ×

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:

rs3748067

IL17A

0.040

GeneticVariation

BEFREE

Thus, IL-17A rs3748067 and rs8193037 might be recommended as a predictor for susceptibility of CAD for Asians.

27376313

2016

dbSNP:

rs3748067

IL17A

0.040

GeneticVariation

BEFREE

This study examined the potential association between CAD and five SNPs (rs8193037, rs8193036, rs3819024, rs2275913, and rs3748067) of the IL17A gene.

27525938

2016

dbSNP:

rs3748067

IL17A

0.040

GeneticVariation

BEFREE

Logistic regression analysis revealed that CC [odds ratio (OR) = 3.81, 95% confidence interval (CI) = 2.11-7.16] and TC+CC (OR = 1.54, 95%CI = 1.11-2.14) rs3748067 genotypes were associated with an increased risk of CAD compared to the TT variant.

26909948

2016

dbSNP:

rs3748067

IL17A

0.040

GeneticVariation

BEFREE

We conducted a case-control study to estimate the association between IL-17A rs2275913, rs3819025 and rs3748067 polymorphisms and development of coronary artery disease.

26617905

2015