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rs12229663

From SNPedia

Orientationplus
Stabilizedplus
Make rs12229663(A;A)
Make rs12229663(A;G)
Make rs12229663(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position70856216
GenePTPRR
is asnp
is mentioned by
dbSNPrs12229663
ebirs12229663
HLIrs12229663
Exacrs12229663
Varsomers12229663
Maprs12229663
PheGenIrs12229663
hapmaprs12229663
1000 genomesrs12229663
hgdprs12229663
ensemblrs12229663
gopubmedrs12229663
geneviewrs12229663
scholarrs12229663
googlers12229663
pharmgkbrs12229663
gwascentralrs12229663
openSNPrs12229663
23andMers12229663
23andMe allrs12229663
SNP Nexus

SNPshotrs12229663
SNPdbers12229663
MSV3drs12229663
GWAS Ctlgrs12229663
GMAF0.2498
Max Magnitude
? (A;A) (A;G) (G;G) 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 G
P-val 5E-9
Odds Ratio .10 [0.066-0.132] unit increase