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rs11662748

From SNPedia

Orientationplus
Stabilizedplus
Make rs11662748(A;A)
Make rs11662748(A;G)
Make rs11662748(G;G)
ReferenceGRCh38 38.1/142
Chromosome18
Position5762619
GeneMIR3976HG
is asnp
is mentioned by
dbSNPrs11662748
ebirs11662748
HLIrs11662748
Exacrs11662748
Varsomers11662748
Maprs11662748
PheGenIrs11662748
hapmaprs11662748
1000 genomesrs11662748
hgdprs11662748
ensemblrs11662748
gopubmedrs11662748
geneviewrs11662748
scholarrs11662748
googlers11662748
pharmgkbrs11662748
gwascentralrs11662748
openSNPrs11662748
23andMers11662748
23andMe allrs11662748
SNP Nexus

SNPshotrs11662748
SNPdbers11662748
MSV3drs11662748
GWAS Ctlgrs11662748
Max Magnitude
? (A;A) (A;G) (G;G) 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 1E-6
Odds Ratio .03 [NR] min/d increase