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rs12038826

From SNPedia

Orientationplus
Stabilizedplus
Make rs12038826(C;C)
Make rs12038826(C;T)
Make rs12038826(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position230787205
GeneCAPN9
is asnp
is mentioned by
dbSNPrs12038826
ebirs12038826
HLIrs12038826
Exacrs12038826
Varsomers12038826
Maprs12038826
PheGenIrs12038826
hapmaprs12038826
1000 genomesrs12038826
hgdprs12038826
ensemblrs12038826
gopubmedrs12038826
geneviewrs12038826
scholarrs12038826
googlers12038826
pharmgkbrs12038826
gwascentralrs12038826
openSNPrs12038826
23andMers12038826
23andMe allrs12038826
SNP Nexus

SNPshotrs12038826
SNPdbers12038826
MSV3drs12038826
GWAS Ctlgrs12038826
GMAF0.06749
Max Magnitude
? (C;C) (C;T) (T;T) 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 7E-6
Odds Ratio NR NR