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rs10160399

From SNPedia

Orientationplus
Stabilizedplus
Make rs10160399(C;C)
Make rs10160399(C;T)
Make rs10160399(T;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position4495346
is asnp
is mentioned by
dbSNPrs10160399
ebirs10160399
HLIrs10160399
Exacrs10160399
Varsomers10160399
Maprs10160399
PheGenIrs10160399
hapmaprs10160399
1000 genomesrs10160399
hgdprs10160399
ensemblrs10160399
gopubmedrs10160399
geneviewrs10160399
scholarrs10160399
googlers10160399
pharmgkbrs10160399
gwascentralrs10160399
openSNPrs10160399
23andMers10160399
23andMe allrs10160399
SNP Nexus

SNPshotrs10160399
SNPdbers10160399
MSV3drs10160399
GWAS Ctlgrs10160399
Max Magnitude
? (C;C) (C;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 A
P-val 2E-6
Odds Ratio .03 [NR] mmHg increase