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rs1656966

From SNPedia

Orientationminus
Stabilizedminus
Make rs1656966(C;C)
Make rs1656966(C;T)
Make rs1656966(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position186748463
is asnp
is mentioned by
dbSNPrs1656966
ebirs1656966
HLIrs1656966
Exacrs1656966
Varsomers1656966
Maprs1656966
PheGenIrs1656966
hapmaprs1656966
1000 genomesrs1656966
hgdprs1656966
ensemblrs1656966
gopubmedrs1656966
geneviewrs1656966
scholarrs1656966
googlers1656966
pharmgkbrs1656966
gwascentralrs1656966
openSNPrs1656966
23andMers1656966
23andMe allrs1656966
SNP Nexus

SNPshotrs1656966
SNPdbers1656966
MSV3drs1656966
GWAS Ctlgrs1656966
GMAF0.197
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 4E-21
Odds Ratio NR NR