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rs4773144

From SNPedia

Orientationplus
Stabilizedplus
Make rs4773144(A;A)
Make rs4773144(A;G)
Make rs4773144(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position110308365
GeneCOL4A1, COL4A2
is asnp
is mentioned by
dbSNPrs4773144
ebirs4773144
HLIrs4773144
Exacrs4773144
Varsomers4773144
Maprs4773144
PheGenIrs4773144
hapmaprs4773144
1000 genomesrs4773144
hgdprs4773144
ensemblrs4773144
gopubmedrs4773144
geneviewrs4773144
scholarrs4773144
googlers4773144
pharmgkbrs4773144
gwascentralrs4773144
openSNPrs4773144
23andMers4773144
23andMe allrs4773144
SNP Nexus

SNPshotrs4773144
SNPdbers4773144
MSV3drs4773144
GWAS Ctlgrs4773144
GMAF0.4073
Max Magnitude
? (A;A) (A;G) (G;G) 28
Coronary Heart Disease


[PMID 4021556] Analysis of common and coding variants with cardiovascular disease in the diabetes heart study.

[PMID 3584137] Improvement in Prediction of Coronary Heart Disease Risk over Conventional Risk Factors Using SNPs Identified in Genome-Wide Association Studies.

[PMID 3583714] Risk loci for coronary artery calcification replicated at 9p21 and 6q24 in the Heinz Nixdorf Recall Study

[PMID 3266236OA-icon.png] Genetic Profiling Using Genome-Wide Significant Coronary Artery Disease Risk Variants Does Not Improve the Prediction of Subclinical Atherosclerosis: The Cardiovascular Risk in Young Finns Study, the Bogalusa Heart Study and the Health 2000 Survey – A Meta-Analysis of Three Independent Studies

[PMID 3179381] Thirty-five common variants for coronary artery disease: the fruits of much collaborative labour.

[PMID 3178591] Large-Scale Gene-Centric Analysis Identifies Novel Variants for Coronary Artery Disease.

[PMID 24573017] Associations between the CDKN2A/B, ADTRP and PDGFD Polymorphisms and the Development of Coronary Atherosclerosis in Japanese Patients.

[PMID 23202125OA-icon.png] Large-scale association analysis identifies new risk loci for coronary artery disease.

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 G
P-val 2E-6
Odds Ratio 1.08 [1.05-1.12]
GWAS snp
PMID [PMID 21378990OA-icon.png]
Trait Coronary heart disease
Title Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
Risk Allele G
P-val 4E-9
Odds Ratio 1.0700 [1.05-1.09]