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rs12525668

From SNPedia

Orientationplus
Stabilizedplus
Make rs12525668(A;A)
Make rs12525668(A;G)
Make rs12525668(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position107696467
is asnp
is mentioned by
dbSNPrs12525668
ebirs12525668
HLIrs12525668
Exacrs12525668
Varsomers12525668
Maprs12525668
PheGenIrs12525668
hapmaprs12525668
1000 genomesrs12525668
hgdprs12525668
ensemblrs12525668
gopubmedrs12525668
geneviewrs12525668
scholarrs12525668
googlers12525668
pharmgkbrs12525668
gwascentralrs12525668
openSNPrs12525668
23andMers12525668
23andMe allrs12525668
SNP Nexus

SNPshotrs12525668
SNPdbers12525668
MSV3drs12525668
GWAS Ctlgrs12525668
GMAF0.07943
Max Magnitude
? (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 8E-11
Odds Ratio NR NR