Have questions? Visit https://www.reddit.com/r/SNPedia

rs9536591

From SNPedia

Orientationplus
Stabilizedplus
Make rs9536591(A;A)
Make rs9536591(A;C)
Make rs9536591(C;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position54006952
is asnp
is mentioned by
dbSNPrs9536591
ebirs9536591
HLIrs9536591
Exacrs9536591
Varsomers9536591
Maprs9536591
PheGenIrs9536591
hapmaprs9536591
1000 genomesrs9536591
hgdprs9536591
ensemblrs9536591
gopubmedrs9536591
geneviewrs9536591
scholarrs9536591
googlers9536591
pharmgkbrs9536591
gwascentralrs9536591
openSNPrs9536591
23andMers9536591
23andMe allrs9536591
SNP Nexus

SNPshotrs9536591
SNPdbers9536591
MSV3drs9536591
GWAS Ctlgrs9536591
GMAF0.4972
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS
SNP rs9536591
PubMedID [PMID 17434096OA-icon.png]
Condition Stroke
Gene Intergenic
Risk Allele
pValue 6.00E-006
OR 1.92
95% CI 1.41-2.63



GET Evidence
rs9536591
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.40625
summary