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rs9351814

From SNPedia

Orientationplus
Stabilizedplus
Make rs9351814(A;A)
Make rs9351814(A;C)
Make rs9351814(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position71484004
is asnp
is mentioned by
dbSNPrs9351814
ebirs9351814
HLIrs9351814
Exacrs9351814
Varsomers9351814
Maprs9351814
PheGenIrs9351814
hapmaprs9351814
1000 genomesrs9351814
hgdprs9351814
ensemblrs9351814
gopubmedrs9351814
geneviewrs9351814
scholarrs9351814
googlers9351814
pharmgkbrs9351814
gwascentralrs9351814
openSNPrs9351814
23andMers9351814
23andMe allrs9351814
SNP Nexus

SNPshotrs9351814
SNPdbers9351814
MSV3drs9351814
GWAS Ctlgrs9351814
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 24262325OA-icon.png]
Trait Coronary artery disease or ischemic stroke
Title Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants.
Risk Allele
P-val 5E-8
Odds Ratio NR NR