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rs12263766

From SNPedia

Orientationplus
Stabilizedplus
Make rs12263766(A;A)
Make rs12263766(A;G)
Make rs12263766(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position9955027
is asnp
is mentioned by
dbSNPrs12263766
dbSNP (classic)rs12263766
ClinGenrs12263766
ebirs12263766
HLIrs12263766
Exacrs12263766
Gnomadrs12263766
Varsomers12263766
LitVarrs12263766
Maprs12263766
PheGenIrs12263766
Biobankrs12263766
1000 genomesrs12263766
hgdprs12263766
ensemblrs12263766
geneviewrs12263766
scholarrs12263766
googlers12263766
pharmgkbrs12263766
gwascentralrs12263766
openSNPrs12263766
23andMers12263766
SNPshotrs12263766
SNPdbers12263766
MSV3drs12263766
GWAS Ctlgrs12263766
GMAF0.01102
Max Magnitude0
? (A;A) (A;G) (G;G) 28


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 G
P-val 3E-6
Odds Ratio .02 [NR] nmol/d increase