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rs7762246

From SNPedia

Orientationplus
Stabilizedplus
Make rs7762246(C;C)
Make rs7762246(C;T)
Make rs7762246(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position51234458
is asnp
is mentioned by
dbSNPrs7762246
dbSNP (classic)rs7762246
ClinGenrs7762246
ebirs7762246
HLIrs7762246
Exacrs7762246
Gnomadrs7762246
Varsomers7762246
LitVarrs7762246
Maprs7762246
PheGenIrs7762246
Biobankrs7762246
1000 genomesrs7762246
hgdprs7762246
ensemblrs7762246
geneviewrs7762246
scholarrs7762246
googlers7762246
pharmgkbrs7762246
gwascentralrs7762246
openSNPrs7762246
23andMers7762246
SNPshotrs7762246
SNPdbers7762246
MSV3drs7762246
GWAS Ctlgrs7762246
GMAF0.09229
Max Magnitude0
? (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 6E-6
Odds Ratio .03 [NR] min/d increase