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rs974819

From SNPedia

Orientationminus
Stabilizedminus
Make rs974819(A;A)
Make rs974819(A;G)
Make rs974819(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position103789839
is asnp
is mentioned by
dbSNPrs974819
ebirs974819
HLIrs974819
Exacrs974819
Varsomers974819
Maprs974819
PheGenIrs974819
hapmaprs974819
1000 genomesrs974819
hgdprs974819
ensemblrs974819
gopubmedrs974819
geneviewrs974819
scholarrs974819
googlers974819
pharmgkbrs974819
gwascentralrs974819
openSNPrs974819
23andMers974819
23andMe allrs974819
SNP Nexus

SNPshotrs974819
SNPdbers974819
MSV3drs974819
GWAS Ctlgrs974819
GMAF0.4183
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21378988]
Trait Coronary heart disease
Title A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease
Risk Allele T
P-val 2E-9
Odds Ratio 1.0700 [1.04-1.09]

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

[PMID 23364394] A genome-wide association study of a coronary artery disease risk variant

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

[PMID 22704460] A case-control study provides evidence of association for a common SNP rs974819 in PDGFD to coronary heart disease and suggests a sex-dependent effect


[PMID 27585990] PDGF-D gene polymorphism is associated with increased cardiovascular mortality in elderly men.