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rs10486776

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common on affy axiom data
Make rs10486776(A;A)
Make rs10486776(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position15703161
GeneRPL36AP26
is asnp
is mentioned by
dbSNPrs10486776
ebirs10486776
HLIrs10486776
Exacrs10486776
Varsomers10486776
Maprs10486776
PheGenIrs10486776
hapmaprs10486776
1000 genomesrs10486776
hgdprs10486776
ensemblrs10486776
gopubmedrs10486776
geneviewrs10486776
scholarrs10486776
googlers10486776
pharmgkbrs10486776
gwascentralrs10486776
openSNPrs10486776
23andMers10486776
23andMe allrs10486776
SNP Nexus

SNPshotrs10486776
SNPdbers10486776
MSV3drs10486776
GWAS Ctlgrs10486776
GMAF0.07576
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS
SNP rs10486776
PubMedID [PMID 17434096OA-icon.png]
Condition Stroke
Gene Intergenic
Risk Allele
pValue 6.00E-006
OR 5.62
95% CI 2.66-11.9



[PMID 19910543] Confirmation of genomewide association signals in Chinese Han population reveals risk loci for ischemic stroke.


GET Evidence
rs10486776
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.046875
summary