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rs1333047

From SNPedia

Orientationplus
Stabilizedplus
Make rs1333047(A;A)
Make rs1333047(A;T)
Make rs1333047(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position22124505
is asnp
is mentioned by
dbSNPrs1333047
dbSNP (classic)rs1333047
ClinGenrs1333047
ebirs1333047
HLIrs1333047
Exacrs1333047
Gnomadrs1333047
Varsomers1333047
LitVarrs1333047
Maprs1333047
PheGenIrs1333047
Biobankrs1333047
1000 genomesrs1333047
hgdprs1333047
ensemblrs1333047
geneviewrs1333047
scholarrs1333047
googlers1333047
pharmgkbrs1333047
gwascentralrs1333047
openSNPrs1333047
23andMers1333047
SNPshotrs1333047
SNPdbers1333047
MSV3drs1333047
GWAS Ctlgrs1333047
Max Magnitude0
? (A;A) (A;T) (T;T) 28


GWAS snp
PMID [PMID 24262325OA-icon.png]
Trait Large artery stroke
Title Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants.
Risk Allele T
P-val 2E-7
Odds Ratio 1.20 [1.11-1.29]


[PMID 25724239] Sequence Variants on Chromosome 9p21 are Associated with Ischemic Stroke and the Lipids Level in Chinese Han Population


[PMID 28502497] The 9p21.3 locus and cardiovascular risk in familial hypercholesterolemia.