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rs7939886

From SNPedia

Orientationplus
Stabilizedplus
Make rs7939886(G;G)
Make rs7939886(G;T)
Make rs7939886(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position56474785
is asnp
is mentioned by
dbSNPrs7939886
ebirs7939886
HLIrs7939886
Exacrs7939886
Varsomers7939886
Maprs7939886
PheGenIrs7939886
hapmaprs7939886
1000 genomesrs7939886
hgdprs7939886
ensemblrs7939886
gopubmedrs7939886
geneviewrs7939886
scholarrs7939886
googlers7939886
pharmgkbrs7939886
gwascentralrs7939886
openSNPrs7939886
23andMers7939886
23andMe allrs7939886
SNP Nexus

SNPshotrs7939886
SNPdbers7939886
MSV3drs7939886
GWAS Ctlgrs7939886
GMAF0.1185
Max Magnitude
? (G;G) (G;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 2E-7
Odds Ratio NR NR