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rs602633

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A)
(A;C)
(C;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position109278889
is asnp
is mentioned by
dbSNPrs602633
dbSNP (classic)rs602633
ClinGenrs602633
ebirs602633
HLIrs602633
Exacrs602633
Gnomadrs602633
Varsomers602633
LitVarrs602633
Maprs602633
PheGenIrs602633
Biobankrs602633
1000 genomesrs602633
hgdprs602633
ensemblrs602633
geneviewrs602633
scholarrs602633
googlers602633
pharmgkbrs602633
gwascentralrs602633
openSNPrs602633
23andMers602633
SNPshotrs602633
SNPdbers602633
MSV3drs602633
GWAS Ctlgrs602633
Max Magnitude0
? (A;A) (A;C) (C;C) 28


[PMID 2320212] Large-scale association analysis identifies new risk loci for coronary artery disease.

[PMID 18262040OA-icon.png] LDL-cholesterol concentrations: a genome-wide association study

GWAS snp
PMID [PMID 24262325OA-icon.png]
Trait Coronary artery disease
Title Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants.
Risk Allele T
P-val 1E-8
Odds Ratio 1.11 [1.08-1.15]


[PMID 32685059OA-icon.png] Association Study of Coronary Artery Disease-Associated Genome-Wide Significant SNPs with Coronary Stenosis in Pakistani Population.