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rs7634528

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0
Make rs7634528(G;G)
Make rs7634528(G;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position178048676
is asnp
is mentioned by
dbSNPrs7634528
ebirs7634528
HLIrs7634528
Exacrs7634528
Varsomers7634528
Maprs7634528
PheGenIrs7634528
hapmaprs7634528
1000 genomesrs7634528
hgdprs7634528
ensemblrs7634528
gopubmedrs7634528
geneviewrs7634528
scholarrs7634528
googlers7634528
pharmgkbrs7634528
gwascentralrs7634528
openSNPrs7634528
23andMers7634528
23andMe allrs7634528
SNP Nexus

SNPshotrs7634528
SNPdbers7634528
MSV3drs7634528
GWAS Ctlgrs7634528
GMAF0.02112
Max Magnitude0
? (G;G) (G;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 1E-6
Odds Ratio NR NR