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rs1668357

From SNPedia

Orientationminus
Stabilizedminus
Make rs1668357(A;A)
Make rs1668357(A;C)
Make rs1668357(C;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position37964804
is asnp
is mentioned by
dbSNPrs1668357
ebirs1668357
HLIrs1668357
Exacrs1668357
Varsomers1668357
Maprs1668357
PheGenIrs1668357
hapmaprs1668357
1000 genomesrs1668357
hgdprs1668357
ensemblrs1668357
gopubmedrs1668357
geneviewrs1668357
scholarrs1668357
googlers1668357
pharmgkbrs1668357
gwascentralrs1668357
openSNPrs1668357
23andMers1668357
23andMe allrs1668357
SNP Nexus

SNPshotrs1668357
SNPdbers1668357
MSV3drs1668357
GWAS Ctlgrs1668357
GMAF0.1754
Max Magnitude
? (A;A) (A;C) (C;C) 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 4E-8
Odds Ratio NR NR