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rs12803066

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;G) 2.5 increased risk of myopia
Make rs12803066(A;A)
Make rs12803066(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position100172688
GeneCNTN5
is asnp
is mentioned by
dbSNPrs12803066
ebirs12803066
HLIrs12803066
Exacrs12803066
Varsomers12803066
Maprs12803066
PheGenIrs12803066
hapmaprs12803066
1000 genomesrs12803066
hgdprs12803066
ensemblrs12803066
gopubmedrs12803066
geneviewrs12803066
scholarrs12803066
googlers12803066
pharmgkbrs12803066
gwascentralrs12803066
openSNPrs12803066
23andMers12803066
23andMe allrs12803066
SNP Nexus

SNPshotrs12803066
SNPdbers12803066
MSV3drs12803066
GWAS Ctlgrs12803066
GMAF0.1442
Max Magnitude2.5
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23049088]
Trait Myopia (pathological)
Title A Genome-Wide Association Study Provides Evidence for Association of Chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with High Myopia in the French Population.
Risk Allele
P-val 4E-6
Odds Ratio NR NR