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rs11731298

From SNPedia

Orientationplus
Stabilizedplus
Make rs11731298(C;C)
Make rs11731298(C;T)
Make rs11731298(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position147691337
is asnp
is mentioned by
dbSNPrs11731298
dbSNP (classic)rs11731298
ClinGenrs11731298
ebirs11731298
HLIrs11731298
Exacrs11731298
Gnomadrs11731298
Varsomers11731298
LitVarrs11731298
Maprs11731298
PheGenIrs11731298
Biobankrs11731298
1000 genomesrs11731298
hgdprs11731298
ensemblrs11731298
geneviewrs11731298
scholarrs11731298
googlers11731298
pharmgkbrs11731298
gwascentralrs11731298
openSNPrs11731298
23andMers11731298
SNPshotrs11731298
SNPdbers11731298
MSV3drs11731298
GWAS Ctlgrs11731298
GMAF0.06657
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 A
P-val 9E-6
Odds Ratio .03 [NR] pg/mL increase