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rs13407662

From SNPedia

Orientationplus
Stabilizedplus
Make rs13407662(C;C)
Make rs13407662(C;T)
Make rs13407662(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position53555422
is asnp
is mentioned by
dbSNPrs13407662
ebirs13407662
HLIrs13407662
Exacrs13407662
Varsomers13407662
Maprs13407662
PheGenIrs13407662
hapmaprs13407662
1000 genomesrs13407662
hgdprs13407662
ensemblrs13407662
gopubmedrs13407662
geneviewrs13407662
scholarrs13407662
googlers13407662
pharmgkbrs13407662
gwascentralrs13407662
openSNPrs13407662
23andMers13407662
23andMe allrs13407662
SNP Nexus

SNPshotrs13407662
SNPdbers13407662
MSV3drs13407662
GWAS Ctlgrs13407662
GMAF0.03857
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23041239OA-icon.png]
Trait Stroke (ischemic)
Title Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies.
Risk Allele T
P-val 5E-8
Odds Ratio 1.95 [1.53-2.48]