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rs4972489

From SNPedia

Orientationplus
Stabilizedplus
Make rs4972489(A;A)
Make rs4972489(A;C)
Make rs4972489(C;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position175869870
is asnp
is mentioned by
dbSNPrs4972489
dbSNP (classic)rs4972489
ClinGenrs4972489
ebirs4972489
HLIrs4972489
Exacrs4972489
Gnomadrs4972489
Varsomers4972489
LitVarrs4972489
Maprs4972489
PheGenIrs4972489
Biobankrs4972489
1000 genomesrs4972489
hgdprs4972489
ensemblrs4972489
geneviewrs4972489
scholarrs4972489
googlers4972489
pharmgkbrs4972489
gwascentralrs4972489
openSNPrs4972489
23andMers4972489
SNPshotrs4972489
SNPdbers4972489
MSV3drs4972489
GWAS Ctlgrs4972489
GMAF0.2066
Max Magnitude0
? (A;A) (A;C) (C;C) 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 C
P-val 8E-6
Odds Ratio .03 [NR] g/d increase