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rs6099847

From SNPedia

Orientationplus
Stabilizedplus
Make rs6099847(C;C)
Make rs6099847(C;T)
Make rs6099847(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position57926923
is asnp
is mentioned by
dbSNPrs6099847
dbSNP (classic)rs6099847
ClinGenrs6099847
ebirs6099847
HLIrs6099847
Exacrs6099847
Gnomadrs6099847
Varsomers6099847
LitVarrs6099847
Maprs6099847
PheGenIrs6099847
Biobankrs6099847
1000 genomesrs6099847
hgdprs6099847
ensemblrs6099847
geneviewrs6099847
scholarrs6099847
googlers6099847
pharmgkbrs6099847
gwascentralrs6099847
openSNPrs6099847
23andMers6099847
SNPshotrs6099847
SNPdbers6099847
MSV3drs6099847
GWAS Ctlgrs6099847
GMAF0.259
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 7E-6
Odds Ratio .03 [NR] %energy increase