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rs13382811

From SNPedia

Orientationplus
Stabilizedplus
Make rs13382811(C;C)
Make rs13382811(C;T)
Make rs13382811(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position144466053
GeneZEB2
is asnp
is mentioned by
dbSNPrs13382811
ebirs13382811
HLIrs13382811
Exacrs13382811
Varsomers13382811
Maprs13382811
PheGenIrs13382811
hapmaprs13382811
1000 genomesrs13382811
hgdprs13382811
ensemblrs13382811
gopubmedrs13382811
geneviewrs13382811
scholarrs13382811
googlers13382811
pharmgkbrs13382811
gwascentralrs13382811
openSNPrs13382811
23andMers13382811
23andMe allrs13382811
SNP Nexus

SNPshotrs13382811
SNPdbers13382811
MSV3drs13382811
GWAS Ctlgrs13382811
GMAF0.2098
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23933737]
Trait Myopia (severe)
Title Genome-wide association study identifies ZFHX1B as a susceptibility locus for severe myopia.
Risk Allele T
P-val 6E-10
Odds Ratio 1.26 [NR]