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rs10747502

From SNPedia

Orientationplus
Stabilizedplus
Make rs10747502(A;A)
Make rs10747502(A;G)
Make rs10747502(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position99058491
GenePDE6G
is asnp
is mentioned by
dbSNPrs10747502
ebirs10747502
HLIrs10747502
Exacrs10747502
Varsomers10747502
Maprs10747502
PheGenIrs10747502
hapmaprs10747502
1000 genomesrs10747502
hgdprs10747502
ensemblrs10747502
gopubmedrs10747502
geneviewrs10747502
scholarrs10747502
googlers10747502
pharmgkbrs10747502
gwascentralrs10747502
openSNPrs10747502
23andMers10747502
23andMe allrs10747502
SNP Nexus

SNPshotrs10747502
SNPdbers10747502
MSV3drs10747502
GWAS Ctlgrs10747502
GMAF0.112
Max Magnitude
? (A;A) (A;G) (G;G) 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-9
Odds Ratio NR NR
GWAS snp
PMID [PMID 23251661OA-icon.png]
Trait Obesity-related traits
Title Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population.
Risk Allele A
P-val 5E-7
Odds Ratio .04 [NR]  %awake time increase