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rs1559777

From SNPedia

Orientationminus
Stabilizedplus
Make rs1559777(C;C)
Make rs1559777(C;T)
Make rs1559777(T;T)
ReferenceGRCh38 38.1/142
Chromosome15
Position57788419
is asnp
is mentioned by
dbSNPrs1559777
ebirs1559777
HLIrs1559777
Exacrs1559777
Varsomers1559777
Maprs1559777
PheGenIrs1559777
hapmaprs1559777
1000 genomesrs1559777
hgdprs1559777
ensemblrs1559777
gopubmedrs1559777
geneviewrs1559777
scholarrs1559777
googlers1559777
pharmgkbrs1559777
gwascentralrs1559777
openSNPrs1559777
23andMers1559777
23andMe allrs1559777
SNP Nexus

SNPshotrs1559777
SNPdbers1559777
MSV3drs1559777
GWAS Ctlgrs1559777
GMAF0.2769
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-6
Odds Ratio NR NR