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rs10274279

From SNPedia

Orientationplus
Stabilizedplus
Make rs10274279(C;C)
Make rs10274279(C;T)
Make rs10274279(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position157594749
GenePTPRN2
is asnp
is mentioned by
dbSNPrs10274279
ebirs10274279
HLIrs10274279
Exacrs10274279
Varsomers10274279
Maprs10274279
PheGenIrs10274279
hapmaprs10274279
1000 genomesrs10274279
hgdprs10274279
ensemblrs10274279
gopubmedrs10274279
geneviewrs10274279
scholarrs10274279
googlers10274279
pharmgkbrs10274279
gwascentralrs10274279
openSNPrs10274279
23andMers10274279
23andMe allrs10274279
SNP Nexus

SNPshotrs10274279
SNPdbers10274279
MSV3drs10274279
GWAS Ctlgrs10274279
GMAF0.1433
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 4E-11
Odds Ratio NR NR