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rs10486201

From SNPedia

Orientationplus
Stabilizedplus
Make rs10486201(C;C)
Make rs10486201(C;T)
Make rs10486201(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position7898965
is asnp
is mentioned by
dbSNPrs10486201
ebirs10486201
HLIrs10486201
Exacrs10486201
Varsomers10486201
Maprs10486201
PheGenIrs10486201
hapmaprs10486201
1000 genomesrs10486201
hgdprs10486201
ensemblrs10486201
gopubmedrs10486201
geneviewrs10486201
scholarrs10486201
googlers10486201
pharmgkbrs10486201
gwascentralrs10486201
openSNPrs10486201
23andMers10486201
23andMe allrs10486201
SNP Nexus

SNPshotrs10486201
SNPdbers10486201
MSV3drs10486201
GWAS Ctlgrs10486201
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 6E-6
Odds Ratio .03 [NR] min/d increase