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rs999556

From SNPedia

Orientationplus
Stabilizedplus
Make rs999556(A;A)
Make rs999556(A;G)
Make rs999556(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position151094113
is asnp
is mentioned by
dbSNPrs999556
ebirs999556
HLIrs999556
Exacrs999556
Varsomers999556
Maprs999556
PheGenIrs999556
hapmaprs999556
1000 genomesrs999556
hgdprs999556
ensemblrs999556
gopubmedrs999556
geneviewrs999556
scholarrs999556
googlers999556
pharmgkbrs999556
gwascentralrs999556
openSNPrs999556
23andMers999556
23andMe allrs999556
SNP Nexus

SNPshotrs999556
SNPdbers999556
MSV3drs999556
GWAS Ctlgrs999556
GMAF0.4775
Max Magnitude
? (A;A) (A;G) (G;G) 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-15
Odds Ratio NR NR