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rs1011397

From SNPedia

Orientationplus
Stabilizedplus
Make rs1011397(C;C)
Make rs1011397(C;T)
Make rs1011397(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position143932550
is asnp
is mentioned by
dbSNPrs1011397
ebirs1011397
HLIrs1011397
Exacrs1011397
Varsomers1011397
Maprs1011397
PheGenIrs1011397
hapmaprs1011397
1000 genomesrs1011397
hgdprs1011397
ensemblrs1011397
gopubmedrs1011397
geneviewrs1011397
scholarrs1011397
googlers1011397
pharmgkbrs1011397
gwascentralrs1011397
openSNPrs1011397
23andMers1011397
23andMe allrs1011397
SNP Nexus

SNPshotrs1011397
SNPdbers1011397
MSV3drs1011397
GWAS Ctlgrs1011397
GMAF0.2227
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 G
P-val 8E-6
Odds Ratio .04 [NR] kcal/d increase