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rs12449964

From SNPedia

Orientationplus
Stabilizedplus
Make rs12449964(C;C)
Make rs12449964(C;T)
Make rs12449964(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position17641390
is asnp
is mentioned by
dbSNPrs12449964
ebirs12449964
HLIrs12449964
Exacrs12449964
Varsomers12449964
Maprs12449964
PheGenIrs12449964
hapmaprs12449964
1000 genomesrs12449964
hgdprs12449964
ensemblrs12449964
gopubmedrs12449964
geneviewrs12449964
scholarrs12449964
googlers12449964
pharmgkbrs12449964
gwascentralrs12449964
openSNPrs12449964
23andMers12449964
23andMe allrs12449964
SNP Nexus

SNPshotrs12449964
SNPdbers12449964
MSV3drs12449964
GWAS Ctlgrs12449964
Max Magnitude
? (C;C) (C;T) (T;T) 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 2E-8
Odds Ratio NR NR