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rs11838472

From SNPedia

Orientationplus
Stabilizedplus
Make rs11838472(C;C)
Make rs11838472(C;T)
Make rs11838472(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position73167012
is asnp
is mentioned by
dbSNPrs11838472
ebirs11838472
HLIrs11838472
Exacrs11838472
Varsomers11838472
Maprs11838472
PheGenIrs11838472
hapmaprs11838472
1000 genomesrs11838472
hgdprs11838472
ensemblrs11838472
gopubmedrs11838472
geneviewrs11838472
scholarrs11838472
googlers11838472
pharmgkbrs11838472
gwascentralrs11838472
openSNPrs11838472
23andMers11838472
23andMe allrs11838472
SNP Nexus

SNPshotrs11838472
SNPdbers11838472
MSV3drs11838472
GWAS Ctlgrs11838472
GMAF0.1667
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-17
Odds Ratio NR NR