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rs556621

From SNPedia

Orientationminus
Stabilizedminus
Make rs556621(A;A)
Make rs556621(A;C)
Make rs556621(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position44626422
is asnp
is mentioned by
dbSNPrs556621
ebirs556621
HLIrs556621
Exacrs556621
Varsomers556621
Maprs556621
PheGenIrs556621
hapmaprs556621
1000 genomesrs556621
hgdprs556621
ensemblrs556621
gopubmedrs556621
geneviewrs556621
scholarrs556621
googlers556621
pharmgkbrs556621
gwascentralrs556621
openSNPrs556621
23andMers556621
23andMe allrs556621
SNP Nexus

SNPshotrs556621
SNPdbers556621
MSV3drs556621
GWAS Ctlgrs556621
GMAF0.3182
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 22941190OA-icon.png]
Trait Stroke (ischemic)
Title Common variants at 6p21.1 are associated with large artery atherosclerotic stroke.
Risk Allele A
P-val 5E-8
Odds Ratio 1.21 [1.13-1.30]


[PMID 27567922] Association of GWAS-Supported Variants rs556621 on Chromosome 6p21.1 with Large Artery Atherosclerotic Stroke in a Southern Chinese Han Population.