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rs939658

From SNPedia

Orientationminus
Stabilizedminus
Make rs939658(C;C)
Make rs939658(C;T)
Make rs939658(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position79159527
is asnp
is mentioned by
dbSNPrs939658
ebirs939658
HLIrs939658
Exacrs939658
Varsomers939658
Maprs939658
PheGenIrs939658
hapmaprs939658
1000 genomesrs939658
hgdprs939658
ensemblrs939658
gopubmedrs939658
geneviewrs939658
scholarrs939658
googlers939658
pharmgkbrs939658
gwascentralrs939658
openSNPrs939658
23andMers939658
23andMe allrs939658
SNP Nexus

SNPshotrs939658
SNPdbers939658
MSV3drs939658
GWAS Ctlgrs939658
GMAF0.4334
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20835236OA-icon.png]
Trait
Title A genome-wide association study for myopia and refractive error identifies a susceptibility locus at 15q25
Risk Allele G
P-val 2E-9
Odds Ratio 0.15 [0.10-0.20] diopter decrease