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rs11653011

From SNPedia

Orientationplus
Stabilizedplus
Make rs11653011(C;C)
Make rs11653011(C;T)
Make rs11653011(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position55442483
is asnp
is mentioned by
dbSNPrs11653011
dbSNP (classic)rs11653011
ClinGenrs11653011
ebirs11653011
HLIrs11653011
Exacrs11653011
Gnomadrs11653011
Varsomers11653011
LitVarrs11653011
Maprs11653011
PheGenIrs11653011
Biobankrs11653011
1000 genomesrs11653011
hgdprs11653011
ensemblrs11653011
geneviewrs11653011
scholarrs11653011
googlers11653011
pharmgkbrs11653011
gwascentralrs11653011
openSNPrs11653011
23andMers11653011
SNPshotrs11653011
SNPdbers11653011
MSV3drs11653011
GWAS Ctlgrs11653011
GMAF0.3792
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 .04 [NR] unit increase