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rs10792665

From SNPedia

Orientationplus
Stabilizedplus
Make rs10792665(G;G)
Make rs10792665(G;T)
Make rs10792665(T;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position82938726
is asnp
is mentioned by
dbSNPrs10792665
ebirs10792665
HLIrs10792665
Exacrs10792665
Varsomers10792665
Maprs10792665
PheGenIrs10792665
hapmaprs10792665
1000 genomesrs10792665
hgdprs10792665
ensemblrs10792665
gopubmedrs10792665
geneviewrs10792665
scholarrs10792665
googlers10792665
pharmgkbrs10792665
gwascentralrs10792665
openSNPrs10792665
23andMers10792665
23andMe allrs10792665
SNP Nexus

SNPshotrs10792665
SNPdbers10792665
MSV3drs10792665
GWAS Ctlgrs10792665
Max Magnitude
? (G;G) (G;T) (T;T) 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 C
P-val 6E-6
Odds Ratio .03 [NR] ng/dL increase