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rs4793501

From SNPedia

Orientationplus
Stabilizedplus
Make rs4793501(C;C)
Make rs4793501(C;T)
Make rs4793501(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position70722593
is asnp
is mentioned by
dbSNPrs4793501
ebirs4793501
HLIrs4793501
Exacrs4793501
Varsomers4793501
Maprs4793501
PheGenIrs4793501
hapmaprs4793501
1000 genomesrs4793501
hgdprs4793501
ensemblrs4793501
gopubmedrs4793501
geneviewrs4793501
scholarrs4793501
googlers4793501
pharmgkbrs4793501
gwascentralrs4793501
openSNPrs4793501
23andMers4793501
23andMe allrs4793501
SNP Nexus

SNPshotrs4793501
SNPdbers4793501
MSV3drs4793501
GWAS Ctlgrs4793501
GMAF0.4284
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 C
P-val 3E-8
Odds Ratio .08 [0.053-0.107] unit increase