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rs4792192

From SNPedia

Orientationplus
Stabilizedplus
Make rs4792192(C;C)
Make rs4792192(C;T)
Make rs4792192(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position11900144
GeneDNAH9
is asnp
is mentioned by
dbSNPrs4792192
ebirs4792192
HLIrs4792192
Exacrs4792192
Varsomers4792192
Maprs4792192
PheGenIrs4792192
hapmaprs4792192
1000 genomesrs4792192
hgdprs4792192
ensemblrs4792192
gopubmedrs4792192
geneviewrs4792192
scholarrs4792192
googlers4792192
pharmgkbrs4792192
gwascentralrs4792192
openSNPrs4792192
23andMers4792192
23andMe allrs4792192
SNP Nexus

SNPshotrs4792192
SNPdbers4792192
MSV3drs4792192
GWAS Ctlgrs4792192
GMAF0.3035
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-6
Odds Ratio NR NR