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rs1656404

From SNPedia

Orientationminus
Stabilizedplus
Make rs1656404(C;C)
Make rs1656404(C;T)
Make rs1656404(T;T)
ReferenceGRCh38 38.1/142
Chromosome2
Position232515231
is asnp
is mentioned by
dbSNPrs1656404
ebirs1656404
HLIrs1656404
Exacrs1656404
Varsomers1656404
Maprs1656404
PheGenIrs1656404
hapmaprs1656404
1000 genomesrs1656404
hgdprs1656404
ensemblrs1656404
gopubmedrs1656404
geneviewrs1656404
scholarrs1656404
googlers1656404
pharmgkbrs1656404
gwascentralrs1656404
openSNPrs1656404
23andMers1656404
23andMe allrs1656404
SNP Nexus

SNPshotrs1656404
SNPdbers1656404
MSV3drs1656404
GWAS Ctlgrs1656404
GMAF0.1511
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23396134OA-icon.png]
Trait Refractive error
Title Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia.
Risk Allele A
P-val 8E-11
Odds Ratio .15 [0.11-0.20] unit decrease