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rs10467147

From SNPedia

Orientationplus
Stabilizedplus
Make rs10467147(A;A)
Make rs10467147(A;G)
Make rs10467147(G;G)
ReferenceGRCh38 38.1/142
Chromosome12
Position40373560
is asnp
is mentioned by
dbSNPrs10467147
ebirs10467147
HLIrs10467147
Exacrs10467147
Varsomers10467147
Maprs10467147
PheGenIrs10467147
hapmaprs10467147
1000 genomesrs10467147
hgdprs10467147
ensemblrs10467147
gopubmedrs10467147
geneviewrs10467147
scholarrs10467147
googlers10467147
pharmgkbrs10467147
gwascentralrs10467147
openSNPrs10467147
23andMers10467147
23andMe allrs10467147
SNP Nexus

SNPshotrs10467147
SNPdbers10467147
MSV3drs10467147
GWAS Ctlgrs10467147
Max Magnitude
? (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 A
P-val 5E-6
Odds Ratio .03 [NR] ng/mL increase