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rs17114036

From SNPedia

Orientationplus
Stabilizedplus
Make rs17114036(A;A)
Make rs17114036(A;G)
Make rs17114036(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position56497149
GenePPAP2B
is asnp
is mentioned by
dbSNPrs17114036
ebirs17114036
HLIrs17114036
Exacrs17114036
Varsomers17114036
Maprs17114036
PheGenIrs17114036
hapmaprs17114036
1000 genomesrs17114036
hgdprs17114036
ensemblrs17114036
gopubmedrs17114036
geneviewrs17114036
scholarrs17114036
googlers17114036
pharmgkbrs17114036
gwascentralrs17114036
openSNPrs17114036
23andMers17114036
23andMe allrs17114036
SNP Nexus

SNPshotrs17114036
SNPdbers17114036
MSV3drs17114036
GWAS Ctlgrs17114036
GMAF0.08953
Max Magnitude
? (A;A) (A;G) (G;G) 28
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 1E-8
Odds Ratio 1.15 [1.1-1.22]
GWAS snp
PMID [PMID 21378990OA-icon.png]
Trait Coronary heart disease
Title Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
Risk Allele A
P-val 4E-19
Odds Ratio 1.1700 [1.13-1.22]

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

[PMID 23161703] Influence of 23 coronary artery disease variants on recurrent myocardial infarction or cardiac death: the GRACE Genetics Study.