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rs4683505

From SNPedia

Orientationplus
Stabilizedplus
Make rs4683505(C;C)
Make rs4683505(C;T)
Make rs4683505(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position140528335
GeneCLSTN2
is asnp
is mentioned by
dbSNPrs4683505
ebirs4683505
HLIrs4683505
Exacrs4683505
Varsomers4683505
Maprs4683505
PheGenIrs4683505
hapmaprs4683505
1000 genomesrs4683505
hgdprs4683505
ensemblrs4683505
gopubmedrs4683505
geneviewrs4683505
scholarrs4683505
googlers4683505
pharmgkbrs4683505
gwascentralrs4683505
openSNPrs4683505
23andMers4683505
23andMe allrs4683505
SNP Nexus

SNPshotrs4683505
SNPdbers4683505
MSV3drs4683505
GWAS Ctlgrs4683505
GMAF0.135
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-7
Odds Ratio NR NR