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rs7128099

From SNPedia

Orientationplus
Stabilizedplus
Make rs7128099(A;A)
Make rs7128099(A;G)
Make rs7128099(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position20334898
is asnp
is mentioned by
dbSNPrs7128099
dbSNP (classic)rs7128099
ClinGenrs7128099
ebirs7128099
HLIrs7128099
Exacrs7128099
Gnomadrs7128099
Varsomers7128099
LitVarrs7128099
Maprs7128099
PheGenIrs7128099
Biobankrs7128099
1000 genomesrs7128099
hgdprs7128099
ensemblrs7128099
geneviewrs7128099
scholarrs7128099
googlers7128099
pharmgkbrs7128099
gwascentralrs7128099
openSNPrs7128099
23andMers7128099
SNPshotrs7128099
SNPdbers7128099
MSV3drs7128099
GWAS Ctlgrs7128099
GMAF0.4146
Max Magnitude0
? (A;A) (A;G) (G;G) 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 .03 [NR] ng/mL increase