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rs10758892

From SNPedia

Orientationplus
Stabilizedplus
Make rs10758892(A;A)
Make rs10758892(A;G)
Make rs10758892(G;G)
ReferenceGRCh37.p5 37.3/137
Chromosome9
Position7734250
is asnp
is mentioned by
dbSNPrs10758892
ebirs10758892
HLIrs10758892
Exacrs10758892
Varsomers10758892
Maprs10758892
PheGenIrs10758892
hapmaprs10758892
1000 genomesrs10758892
hgdprs10758892
ensemblrs10758892
gopubmedrs10758892
geneviewrs10758892
scholarrs10758892
googlers10758892
pharmgkbrs10758892
gwascentralrs10758892
openSNPrs10758892
23andMers10758892
23andMe allrs10758892
SNP Nexus

SNPshotrs10758892
SNPdbers10758892
MSV3drs10758892
GWAS Ctlgrs10758892
GMAF0.1079
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 9E-6
Odds Ratio NR NR