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rs12526453

From SNPedia

Orientationplus
Stabilizedplus
Make rs12526453(C;C)
Make rs12526453(C;G)
Make rs12526453(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position12927312
GenePHACTR1
is asnp
is mentioned by
dbSNPrs12526453
ebirs12526453
HLIrs12526453
Exacrs12526453
Varsomers12526453
Maprs12526453
PheGenIrs12526453
hapmaprs12526453
1000 genomesrs12526453
hgdprs12526453
ensemblrs12526453
gopubmedrs12526453
geneviewrs12526453
scholarrs12526453
googlers12526453
pharmgkbrs12526453
gwascentralrs12526453
openSNPrs12526453
23andMers12526453
23andMe allrs12526453
SNP Nexus

SNPshotrs12526453
SNPdbers12526453
MSV3drs12526453
GWAS Ctlgrs12526453
GMAF0.1905
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 19198609OA-icon.png]
Trait Myocardial infarction (early onset)
Title Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants
Risk Allele C
P-val 1E-9
Odds Ratio 1.12 [1.08-1.17]



GWAS snp
PMID [PMID 21378990OA-icon.png]
Trait
Title Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
Risk Allele C
P-val 1E-9
Odds Ratio 1.1000 [1.06-1.13]


[PMID 22848412OA-icon.png] Genetic Markers Enhance Coronary Risk Prediction in Men: The MORGAM Prospective Cohorts

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

[PMID 20835900OA-icon.png] Genetics of diabetes complications.

[PMID 22152955OA-icon.png] Genetic susceptibility to coronary heart disease in type 2 diabetes: 3 independent studies.


GET Evidence
rs12526453
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.1875
summary



[PMID 23561647] Genome-wide association study of coronary and aortic calcification implicates risk loci for coronary artery disease and myocardial infarction