rs6725887

plus

Geno	Mag	Summary
(T;T)	0

Reference

GRCh38 38.1/141

Chromosome

2

Position

202881162

Gene

0.073

0

(C;C) (C;T) (T;T)

28

SNP Risk Version Effect

GWAS snp
PMID	[PMID 19198609 ]
Trait	Myocardial infarction (early onset)
Title	Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants
Risk Allele	C
P-val	1E-8
Odds Ratio	1.17 [1.11-1.23]

GWAS snp
PMID	[PMID 21378990 ]
Trait
Title	Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
Risk Allele	C
P-val	1E-9
Odds Ratio	1.1400 [1.09-1.19]

[PMID 19956433 ] Genetics of coronary artery disease: focus on genome-wide association studies.

[PMID 20835900 ] Genetics of diabetes complications.

[PMID 21304891 ] A study of CNVs as trait-associated polymorphisms and as expression quantitative trait loci.

GWAS snp
PMID	[PMID 24262325 ]
Trait	Coronary artery disease
Title	Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants.
Risk Allele	C
P-val	2E-8
Odds Ratio	1.14 [1.10-1.19]

[PMID 25804320] Association Between Coronary Artery Disease Genetic Variants and Subclinical Atherosclerosis: an Association Study and Meta-analysis

[PMID 26629484 ] Analysis of rs6725887 in the WD Repeat Protein 12 in Association with Coronary Artery Disease in Iranian Patients.

[PMID 28710368 ] Genome-Wide Linkage Analysis of Large Multiple Multigenerational Families Identifies Novel Genetic Loci for Coronary Artery Disease.