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rs7307902

From SNPedia

Orientationplus
Stabilizedplus
Make rs7307902(C;C)
Make rs7307902(C;T)
Make rs7307902(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position47529233
is asnp
is mentioned by
dbSNPrs7307902
ebirs7307902
HLIrs7307902
Exacrs7307902
Varsomers7307902
Maprs7307902
PheGenIrs7307902
hapmaprs7307902
1000 genomesrs7307902
hgdprs7307902
ensemblrs7307902
gopubmedrs7307902
geneviewrs7307902
scholarrs7307902
googlers7307902
pharmgkbrs7307902
gwascentralrs7307902
openSNPrs7307902
23andMers7307902
23andMe allrs7307902
SNP Nexus

SNPshotrs7307902
SNPdbers7307902
MSV3drs7307902
GWAS Ctlgrs7307902
GMAF0.3384
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 1E-6
Odds Ratio .05 [NR] kcal increase