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rs4142248

From SNPedia

Orientationplus
Stabilizedplus
Make rs4142248(C;C)
Make rs4142248(C;T)
Make rs4142248(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position44384114
GeneZNF285
is asnp
is mentioned by
dbSNPrs4142248
ebirs4142248
HLIrs4142248
Exacrs4142248
Varsomers4142248
Maprs4142248
PheGenIrs4142248
hapmaprs4142248
1000 genomesrs4142248
hgdprs4142248
ensemblrs4142248
gopubmedrs4142248
geneviewrs4142248
scholarrs4142248
googlers4142248
pharmgkbrs4142248
gwascentralrs4142248
openSNPrs4142248
23andMers4142248
23andMe allrs4142248
SNP Nexus

SNPshotrs4142248
SNPdbers4142248
MSV3drs4142248
GWAS Ctlgrs4142248
GMAF0.1093
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-15
Odds Ratio NR NR