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rs1816752

From SNPedia

Orientationminus
Stabilizedminus
Make rs1816752(C;C)
Make rs1816752(C;T)
Make rs1816752(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position24406811
is asnp
is mentioned by
dbSNPrs1816752
dbSNP (classic)rs1816752
ClinGenrs1816752
ebirs1816752
HLIrs1816752
Exacrs1816752
Gnomadrs1816752
Varsomers1816752
LitVarrs1816752
Maprs1816752
PheGenIrs1816752
Biobankrs1816752
1000 genomesrs1816752
hgdprs1816752
ensemblrs1816752
geneviewrs1816752
scholarrs1816752
googlers1816752
pharmgkbrs1816752
gwascentralrs1816752
openSNPrs1816752
23andMers1816752
SNPshotrs1816752
SNPdbers1816752
MSV3drs1816752
GWAS Ctlgrs1816752
GMAF0.3104
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 2E-6
Odds Ratio .05 [NR] nmol/d increase