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rs4839680

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0
Make rs4839680(C;C)
Make rs4839680(C;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position144183185
is asnp
is mentioned by
dbSNPrs4839680
ebirs4839680
HLIrs4839680
Exacrs4839680
Varsomers4839680
Maprs4839680
PheGenIrs4839680
hapmaprs4839680
1000 genomesrs4839680
hgdprs4839680
ensemblrs4839680
gopubmedrs4839680
geneviewrs4839680
scholarrs4839680
googlers4839680
pharmgkbrs4839680
gwascentralrs4839680
openSNPrs4839680
23andMers4839680
23andMe allrs4839680
SNP Nexus

SNPshotrs4839680
SNPdbers4839680
MSV3drs4839680
GWAS Ctlgrs4839680
GMAF0.01745
Max Magnitude0
? (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 1E-15
Odds Ratio NR NR