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rs7665957

From SNPedia

Orientationplus
Stabilizedplus
Make rs7665957(C;C)
Make rs7665957(C;T)
Make rs7665957(T;T)
ReferenceGRCh38 38.1/142
Chromosome4
Position12497263
is asnp
is mentioned by
dbSNPrs7665957
ebirs7665957
HLIrs7665957
Exacrs7665957
Varsomers7665957
Maprs7665957
PheGenIrs7665957
hapmaprs7665957
1000 genomesrs7665957
hgdprs7665957
ensemblrs7665957
gopubmedrs7665957
geneviewrs7665957
scholarrs7665957
googlers7665957
pharmgkbrs7665957
gwascentralrs7665957
openSNPrs7665957
23andMers7665957
23andMe allrs7665957
SNP Nexus

SNPshotrs7665957
SNPdbers7665957
MSV3drs7665957
GWAS Ctlgrs7665957
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 5E-7
Odds Ratio .01 [NR] min/d increase