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rs4841398

From SNPedia

Orientationplus
Stabilizedplus
Make rs4841398(C;C)
Make rs4841398(C;T)
Make rs4841398(T;T)
ReferenceGRCh38 38.1/142
Chromosome8
Position10605296
is asnp
is mentioned by
dbSNPrs4841398
dbSNP (classic)rs4841398
ClinGenrs4841398
ebirs4841398
HLIrs4841398
Exacrs4841398
Gnomadrs4841398
Varsomers4841398
LitVarrs4841398
Maprs4841398
PheGenIrs4841398
Biobankrs4841398
1000 genomesrs4841398
hgdprs4841398
ensemblrs4841398
geneviewrs4841398
scholarrs4841398
googlers4841398
pharmgkbrs4841398
gwascentralrs4841398
openSNPrs4841398
23andMers4841398
SNPshotrs4841398
SNPdbers4841398
MSV3drs4841398
GWAS Ctlgrs4841398
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 3E-6
Odds Ratio .02 [NR] µmol/L increase