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rs12646447

From SNPedia

Orientationplus
Stabilizedplus
Make rs12646447(C;C)
Make rs12646447(C;T)
Make rs12646447(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position110778170
is asnp
is mentioned by
dbSNPrs12646447
dbSNP (old)rs12646447
ClinGenrs12646447
ebirs12646447
HLIrs12646447
Exacrs12646447
Varsomers12646447
Maprs12646447
PheGenIrs12646447
Biobankrs12646447
1000 genomesrs12646447
hgdprs12646447
ensemblrs12646447
gopubmedrs12646447
geneviewrs12646447
scholarrs12646447
googlers12646447
pharmgkbrs12646447
gwascentralrs12646447
openSNPrs12646447
23andMers12646447
23andMe allrs12646447
SNP Nexus

SNPshotrs12646447
SNPdbers12646447
MSV3drs12646447
GWAS Ctlgrs12646447
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 24262325OA-icon.png]
Trait Ischemic stroke
Title Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants.
Risk Allele C
P-val 3E-8
Odds Ratio 1.14 [1.09-1.20]