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rs12190287

From SNPedia

Orientationplus
Stabilizedplus
Make rs12190287(C;C)
Make rs12190287(C;G)
Make rs12190287(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position133893387
GeneLOC100288120, TCF21
is asnp
is mentioned by
dbSNPrs12190287
ebirs12190287
HLIrs12190287
Exacrs12190287
Varsomers12190287
Maprs12190287
PheGenIrs12190287
hapmaprs12190287
1000 genomesrs12190287
hgdprs12190287
ensemblrs12190287
gopubmedrs12190287
geneviewrs12190287
scholarrs12190287
googlers12190287
pharmgkbrs12190287
gwascentralrs12190287
openSNPrs12190287
23andMers12190287
23andMe allrs12190287
SNP Nexus

SNPshotrs12190287
SNPdbers12190287
MSV3drs12190287
GWAS Ctlgrs12190287
GMAF0.3485
Max Magnitude
? (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 23202125OA-icon.png] Large-scale association analysis identifies new risk loci for coronary artery disease.

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

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-9
Odds Ratio 1.11 [1.08-1.15]
GWAS snp
PMID [PMID 21378990OA-icon.png]
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]