rs9982601

Orientation

plus

Stabilized

plus

Make rs9982601(C;C)

Make rs9982601(C;T)

Make rs9982601(T;T)

Reference

GRCh38 38.1/141

Chromosome

21

Position

34226827

is a	snp
is	mentioned by
dbSNP	rs9982601
dbSNP (classic)	rs9982601
ClinGen	rs9982601
ebi	rs9982601
HLI	rs9982601
Exac	rs9982601
Gnomad	rs9982601
Varsome	rs9982601
LitVar	rs9982601
Map	rs9982601
PheGenI	rs9982601
Biobank	rs9982601
1000 genomes	rs9982601
hgdp	rs9982601
ensembl	rs9982601
geneview	rs9982601
scholar	rs9982601
google	rs9982601
pharmgkb	rs9982601
gwascentral	rs9982601
openSNP	rs9982601
23andMe	rs9982601
SNPshot	rs9982601
SNPdbe	rs9982601
MSV3d	rs9982601
GWAS Ctlg	rs9982601

GMAF

0.1088

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

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	T
P-val	3E-10
Odds Ratio	1.18 [1.12-1.24]

GWAS snp
PMID	[PMID 21378990]
Trait
Title	Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
Risk Allele	T
P-val	4E-10
Odds Ratio	1.1800 [1.12-1.24]

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	T
P-val	6E-11
Odds Ratio	1.20 [1.14-1.27]

Coronary Heart Disease

[PMID 23100282] Impact of common genetic variation on response to simvastatin therapy among 18 705 participants in the Heart Protection Study.

[PMID 20835900] Genetics of diabetes complications.

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

[PMID 28458444] Functional Analysis of the Coronary Heart Disease Risk Locus on Chromosome 21q22.