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rs10882165

From SNPedia

Orientationplus
Stabilizedplus
Make rs10882165(A;A)
Make rs10882165(A;T)
Make rs10882165(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position93164567
is asnp
is mentioned by
dbSNPrs10882165
ebirs10882165
HLIrs10882165
Exacrs10882165
Varsomers10882165
Maprs10882165
PheGenIrs10882165
hapmaprs10882165
1000 genomesrs10882165
hgdprs10882165
ensemblrs10882165
gopubmedrs10882165
geneviewrs10882165
scholarrs10882165
googlers10882165
pharmgkbrs10882165
gwascentralrs10882165
openSNPrs10882165
23andMers10882165
23andMe allrs10882165
SNP Nexus

SNPshotrs10882165
SNPdbers10882165
MSV3drs10882165
GWAS Ctlgrs10882165
GMAF0.2888
Max Magnitude
? (A;A) (A;T) (T;T) 28
GWAS snp
PMID [PMID 23396134OA-icon.png]
Trait Refractive error
Title Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia.
Risk Allele T
P-val 1E-11
Odds Ratio .11 [0.076-0.138] unit decrease