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rs8050940

From SNPedia

Orientationplus
Stabilizedplus
Make rs8050940(C;C)
Make rs8050940(C;T)
Make rs8050940(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position62066307
is asnp
is mentioned by
dbSNPrs8050940
ebirs8050940
HLIrs8050940
Exacrs8050940
Varsomers8050940
Maprs8050940
PheGenIrs8050940
hapmaprs8050940
1000 genomesrs8050940
hgdprs8050940
ensemblrs8050940
gopubmedrs8050940
geneviewrs8050940
scholarrs8050940
googlers8050940
pharmgkbrs8050940
gwascentralrs8050940
openSNPrs8050940
23andMers8050940
23andMe allrs8050940
SNP Nexus

SNPshotrs8050940
SNPdbers8050940
MSV3drs8050940
GWAS Ctlgrs8050940
GMAF0.0831
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 1E-26
Odds Ratio NR NR