rs12190287

Orientation

plus

Stabilized

plus

Make rs12190287(C;C)

Make rs12190287(C;G)

Make rs12190287(G;G)

Reference

GRCh38 38.1/141

Chromosome

6

Position

133893387

Gene

TCF21

is a	snp
is	mentioned by
dbSNP	rs12190287
dbSNP (classic)	rs12190287
ClinGen	rs12190287
ebi	rs12190287
HLI	rs12190287
Exac	rs12190287
Gnomad	rs12190287
Varsome	rs12190287
LitVar	rs12190287
Map	rs12190287
PheGenI	rs12190287
Biobank	rs12190287
1000 genomes	rs12190287
hgdp	rs12190287
ensembl	rs12190287
geneview	rs12190287
scholar	rs12190287
google	rs12190287
pharmgkb	rs12190287
gwascentral	rs12190287
openSNP	rs12190287
23andMe	rs12190287
SNPshot	rs12190287
SNPdbe	rs12190287
MSV3d	rs12190287
GWAS Ctlg	rs12190287

GMAF

0.3485

Max Magnitude

0

?	(C;C) (C;G) (G;G)	28

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

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

[PMID 20403199] High-throughput analysis of candidate imprinted genes and allele-specific gene expression in the human term placenta.

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	G
P-val	2E-9
Odds Ratio	1.11 [1.08-1.15]

GWAS snp
PMID	[PMID 21378990]
Trait	Coronary artery disease
Title	Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
Risk Allele	C
P-val	1E-12
Odds Ratio	1.0800 [1.06-1.10]