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rs13201929

From SNPedia

Orientationplus
Stabilizedplus
Make rs13201929(C;C)
Make rs13201929(C;T)
Make rs13201929(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position117284828
is asnp
is mentioned by
dbSNPrs13201929
ebirs13201929
HLIrs13201929
Exacrs13201929
Varsomers13201929
Maprs13201929
PheGenIrs13201929
hapmaprs13201929
1000 genomesrs13201929
hgdprs13201929
ensemblrs13201929
gopubmedrs13201929
geneviewrs13201929
scholarrs13201929
googlers13201929
pharmgkbrs13201929
gwascentralrs13201929
openSNPrs13201929
23andMers13201929
23andMe allrs13201929
SNP Nexus

SNPshotrs13201929
SNPdbers13201929
MSV3drs13201929
GWAS Ctlgrs13201929
GMAF0.1019
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 3E-6
Odds Ratio NR NR