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rs17228212

From SNPedia

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Geno Mag Summary
(C;C) 2 >1.26x increased risk for heart disease
(C;T) 2 1.26x increased risk for heart disease
(T;T) 0 normal
ReferenceGRCh38 38.1/141
Chromosome15
Position67166301
GeneSMAD3
is asnp
is mentioned by
dbSNPrs17228212
dbSNP (classic)rs17228212
ClinGenrs17228212
ebirs17228212
HLIrs17228212
Exacrs17228212
Gnomadrs17228212
Varsomers17228212
LitVarrs17228212
Maprs17228212
PheGenIrs17228212
Biobankrs17228212
1000 genomesrs17228212
hgdprs17228212
ensemblrs17228212
geneviewrs17228212
scholarrs17228212
googlers17228212
pharmgkbrs17228212
gwascentralrs17228212
openSNPrs17228212
23andMers17228212
SNPshotrs17228212
SNPdbers17228212
MSV3drs17228212
GWAS Ctlgrs17228212
GMAF0.1561
Max Magnitude2
? (C;C) (C;T) (T;T) 28


rs17228212 is a SNP found to be associated with heart disease by the German MI (Myocardial infarction) Family Study group in two populations. The odds ratio per allele is 1.26 (CI: 1.11-1.44, p=0.0178).[PMID 17634449OA-icon.png]

[PMID 18979498OA-icon.png] rs599839, rs4970834 and rs17228212 associated with non-HDL cholesterol


[PMID 18780302OA-icon.png] Association studies of 22 candidate SNPs with late-onset Alzheimer's disease.


[PMID 19198609OA-icon.png] Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.


[PMID 19750184OA-icon.png] Genome-wide association studies for atherosclerotic vascular disease and its risk factors.


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


[PMID 20017983OA-icon.png] Evaluation of population impact of candidate polymorphisms for coronary heart disease in the Framingham Heart Study Offspring Cohort.


[PMID 20098575OA-icon.png] Genetics and cardiovascular disease: Design and development of a DNA biobank.


[PMID 21804106OA-icon.png] Comparative analysis of genome-wide association studies signals for lipids, diabetes, and coronary heart disease: Cardiovascular Biomarker Genetics Collaboration.



[PMID 26110764OA-icon.png] Characterization of SMAD3 Gene Variants for Possible Roles in Ventricular Septal Defects and Other Congenital Heart Diseases