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rs13172324

From SNPedia

Orientationplus
Stabilizedplus
Make rs13172324(C;C)
Make rs13172324(C;T)
Make rs13172324(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position7368732
is asnp
is mentioned by
dbSNPrs13172324
ebirs13172324
HLIrs13172324
Exacrs13172324
Varsomers13172324
Maprs13172324
PheGenIrs13172324
hapmaprs13172324
1000 genomesrs13172324
hgdprs13172324
ensemblrs13172324
gopubmedrs13172324
geneviewrs13172324
scholarrs13172324
googlers13172324
pharmgkbrs13172324
gwascentralrs13172324
openSNPrs13172324
23andMers13172324
23andMe allrs13172324
SNP Nexus

SNPshotrs13172324
SNPdbers13172324
MSV3drs13172324
GWAS Ctlgrs13172324
GMAF0.03673
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-10
Odds Ratio NR NR