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rs1472750

From SNPedia

Orientationplus
Stabilizedplus
Make rs1472750(C;C)
Make rs1472750(C;T)
Make rs1472750(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position113475355
is asnp
is mentioned by
dbSNPrs1472750
ebirs1472750
HLIrs1472750
Exacrs1472750
Varsomers1472750
Maprs1472750
PheGenIrs1472750
hapmaprs1472750
1000 genomesrs1472750
hgdprs1472750
ensemblrs1472750
gopubmedrs1472750
geneviewrs1472750
scholarrs1472750
googlers1472750
pharmgkbrs1472750
gwascentralrs1472750
openSNPrs1472750
23andMers1472750
23andMe allrs1472750
SNP Nexus

SNPshotrs1472750
SNPdbers1472750
MSV3drs1472750
GWAS Ctlgrs1472750
GMAF0.06428
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 5E-9
Odds Ratio NR NR