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rs923375

From SNPedia

Orientationplus
Stabilizedplus
Make rs923375(C;C)
Make rs923375(C;T)
Make rs923375(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position3489774
GeneASPA
is asnp
is mentioned by
dbSNPrs923375
ebirs923375
HLIrs923375
Exacrs923375
Varsomers923375
Maprs923375
PheGenIrs923375
hapmaprs923375
1000 genomesrs923375
hgdprs923375
ensemblrs923375
gopubmedrs923375
geneviewrs923375
scholarrs923375
googlers923375
pharmgkbrs923375
gwascentralrs923375
openSNPrs923375
23andMers923375
23andMe allrs923375
SNP Nexus

SNPshotrs923375
SNPdbers923375
MSV3drs923375
GWAS Ctlgrs923375
GMAF0.2594
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-16
Odds Ratio NR NR