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rs11691652

From SNPedia

Orientationplus
Stabilizedplus
Make rs11691652(G;G)
Make rs11691652(G;T)
Make rs11691652(T;T)
ReferenceGRCh38 38.1/142
Chromosome2
Position227720182
is asnp
is mentioned by
dbSNPrs11691652
ebirs11691652
HLIrs11691652
Exacrs11691652
Varsomers11691652
Maprs11691652
PheGenIrs11691652
hapmaprs11691652
1000 genomesrs11691652
hgdprs11691652
ensemblrs11691652
gopubmedrs11691652
geneviewrs11691652
scholarrs11691652
googlers11691652
pharmgkbrs11691652
gwascentralrs11691652
openSNPrs11691652
23andMers11691652
23andMe allrs11691652
SNP Nexus

SNPshotrs11691652
SNPdbers11691652
MSV3drs11691652
GWAS Ctlgrs11691652
Max Magnitude
? (G;G) (G;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 C
P-val 8E-6
Odds Ratio .03 [NR] ng/mL increase