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rs11145465

From SNPedia

Orientationplus
Stabilizedplus
Make rs11145465(A;A)
Make rs11145465(A;C)
Make rs11145465(C;C)
ReferenceGRCh38 38.1/141
Chromosome9
Position69151677
GeneTJP2
is asnp
is mentioned by
dbSNPrs11145465
ebirs11145465
HLIrs11145465
Exacrs11145465
Varsomers11145465
Maprs11145465
PheGenIrs11145465
hapmaprs11145465
1000 genomesrs11145465
hgdprs11145465
ensemblrs11145465
gopubmedrs11145465
geneviewrs11145465
scholarrs11145465
googlers11145465
pharmgkbrs11145465
gwascentralrs11145465
openSNPrs11145465
23andMers11145465
23andMe allrs11145465
SNP Nexus

SNPshotrs11145465
SNPdbers11145465
MSV3drs11145465
GWAS Ctlgrs11145465
GMAF0.1322
Max Magnitude
? (A;A) (A;C) (C;C) 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 A
P-val 7E-9
Odds Ratio .12 [0.083-0.165] unit decrease