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rs2267138

From SNPedia

Orientationplus
Stabilizedplus
Make rs2267138(A;A)
Make rs2267138(A;G)
Make rs2267138(G;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position29397652
is asnp
is mentioned by
dbSNPrs2267138
dbSNP (old)rs2267138
ClinGenrs2267138
ebirs2267138
HLIrs2267138
Exacrs2267138
Gnomadrs2267138
Varsomers2267138
Maprs2267138
PheGenIrs2267138
Biobankrs2267138
1000 genomesrs2267138
hgdprs2267138
ensemblrs2267138
gopubmedrs2267138
geneviewrs2267138
scholarrs2267138
googlers2267138
pharmgkbrs2267138
gwascentralrs2267138
openSNPrs2267138
23andMers2267138
23andMe allrs2267138
SNP Nexus

SNPshotrs2267138
SNPdbers2267138
MSV3drs2267138
GWAS Ctlgrs2267138
GMAF0.1745
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 3E-6
Odds Ratio NR NR