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rs11723530

From SNPedia

Orientationplus
Stabilizedplus
Make rs11723530(A;A)
Make rs11723530(A;G)
Make rs11723530(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position169959732
GeneFOXK1
is asnp
is mentioned by
dbSNPrs11723530
ebirs11723530
HLIrs11723530
Exacrs11723530
Varsomers11723530
Maprs11723530
PheGenIrs11723530
hapmaprs11723530
1000 genomesrs11723530
hgdprs11723530
ensemblrs11723530
gopubmedrs11723530
geneviewrs11723530
scholarrs11723530
googlers11723530
pharmgkbrs11723530
gwascentralrs11723530
openSNPrs11723530
23andMers11723530
23andMe allrs11723530
SNP Nexus

SNPshotrs11723530
SNPdbers11723530
MSV3drs11723530
GWAS Ctlgrs11723530
GMAF0.3039
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 4E-6
Odds Ratio NR NR