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rs4455882

From SNPedia

Orientationplus
Stabilizedplus
Make rs4455882(A;A)
Make rs4455882(A;G)
Make rs4455882(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position120571043
GeneSNTB1
is asnp
is mentioned by
dbSNPrs4455882
ebirs4455882
HLIrs4455882
Exacrs4455882
Varsomers4455882
Maprs4455882
PheGenIrs4455882
hapmaprs4455882
1000 genomesrs4455882
hgdprs4455882
ensemblrs4455882
gopubmedrs4455882
geneviewrs4455882
scholarrs4455882
googlers4455882
pharmgkbrs4455882
gwascentralrs4455882
openSNPrs4455882
23andMers4455882
23andMe allrs4455882
SNP Nexus

SNPshotrs4455882
SNPdbers4455882
MSV3drs4455882
GWAS Ctlgrs4455882
GMAF0.388
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23406873]
Trait Myopia (pathological)
Title A genome-wide meta-analysis identifies two novel loci associated with high myopia in the Han Chinese population.
Risk Allele A
P-val 2E-11
Odds Ratio 1.32 [1.22-1.43]