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rs7311660

From SNPedia

Orientationplus
Stabilizedplus
Make rs7311660(A;A)
Make rs7311660(A;G)
Make rs7311660(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position74660813
is asnp
is mentioned by
dbSNPrs7311660
dbSNP (classic)rs7311660
ClinGenrs7311660
ebirs7311660
HLIrs7311660
Exacrs7311660
Gnomadrs7311660
Varsomers7311660
LitVarrs7311660
Maprs7311660
PheGenIrs7311660
Biobankrs7311660
1000 genomesrs7311660
hgdprs7311660
ensemblrs7311660
geneviewrs7311660
scholarrs7311660
googlers7311660
pharmgkbrs7311660
gwascentralrs7311660
openSNPrs7311660
23andMers7311660
SNPshotrs7311660
SNPdbers7311660
MSV3drs7311660
GWAS Ctlgrs7311660
GMAF0.4789
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 4E-6
Odds Ratio .03 [NR] pg/mL increase