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rs1229542

From SNPedia

Orientationminus
Stabilizedplus
Make rs1229542(A;A)
Make rs1229542(A;C)
Make rs1229542(C;C)
ReferenceGRCh38 38.1/142
Chromosome7
Position97793614
is asnp
is mentioned by
dbSNPrs1229542
ebirs1229542
HLIrs1229542
Exacrs1229542
Varsomers1229542
Maprs1229542
PheGenIrs1229542
hapmaprs1229542
1000 genomesrs1229542
hgdprs1229542
ensemblrs1229542
gopubmedrs1229542
geneviewrs1229542
scholarrs1229542
googlers1229542
pharmgkbrs1229542
gwascentralrs1229542
openSNPrs1229542
23andMers1229542
23andMe allrs1229542
SNP Nexus

SNPshotrs1229542
SNPdbers1229542
MSV3drs1229542
GWAS Ctlgrs1229542
GMAF0.1979
Max Magnitude
? (A;A) (A;C) (C;C) 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 2E-6
Odds Ratio NR NR