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rs6857559

From SNPedia

Orientationplus
Stabilizedplus
Make rs6857559(C;C)
Make rs6857559(C;T)
Make rs6857559(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position188199757
is asnp
is mentioned by
dbSNPrs6857559
ebirs6857559
HLIrs6857559
Exacrs6857559
Varsomers6857559
Maprs6857559
PheGenIrs6857559
hapmaprs6857559
1000 genomesrs6857559
hgdprs6857559
ensemblrs6857559
gopubmedrs6857559
geneviewrs6857559
scholarrs6857559
googlers6857559
pharmgkbrs6857559
gwascentralrs6857559
openSNPrs6857559
23andMers6857559
23andMe allrs6857559
SNP Nexus

SNPshotrs6857559
SNPdbers6857559
MSV3drs6857559
GWAS Ctlgrs6857559
GMAF0.2842
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23049088]
Trait Myopia (pathological)
Title A Genome-Wide Association Study Provides Evidence for Association of Chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with High Myopia in the French Population.
Risk Allele
P-val 3E-21
Odds Ratio NR NR