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rs10053502

From SNPedia

Orientationplus
Stabilizedplus
Make rs10053502(C;C)
Make rs10053502(C;T)
Make rs10053502(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position39979070
is asnp
is mentioned by
dbSNPrs10053502
ebirs10053502
HLIrs10053502
Exacrs10053502
Varsomers10053502
Maprs10053502
PheGenIrs10053502
hapmaprs10053502
1000 genomesrs10053502
hgdprs10053502
ensemblrs10053502
gopubmedrs10053502
geneviewrs10053502
scholarrs10053502
googlers10053502
pharmgkbrs10053502
gwascentralrs10053502
openSNPrs10053502
23andMers10053502
23andMe allrs10053502
SNP Nexus

SNPshotrs10053502
SNPdbers10053502
MSV3drs10053502
GWAS Ctlgrs10053502
GMAF0.073
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 1E-16
Odds Ratio NR NR