rs974819

Orientation

minus

Stabilized

minus

Make rs974819(A;A)

Make rs974819(A;G)

Make rs974819(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

103789839

is a	snp
is	mentioned by
dbSNP	rs974819
dbSNP (classic)	rs974819
ClinGen	rs974819
ebi	rs974819
HLI	rs974819
Exac	rs974819
Gnomad	rs974819
Varsome	rs974819
LitVar	rs974819
Map	rs974819
PheGenI	rs974819
Biobank	rs974819
1000 genomes	rs974819
hgdp	rs974819
ensembl	rs974819
geneview	rs974819
scholar	rs974819
google	rs974819
pharmgkb	rs974819
gwascentral	rs974819
openSNP	rs974819
23andMe	rs974819
SNPshot	rs974819
SNPdbe	rs974819
MSV3d	rs974819
GWAS Ctlg	rs974819

GMAF

0.4183

Max Magnitude

0

?	(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 23202125] 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.