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rs7589998

From SNPedia

Orientationplus
Stabilizedplus
Make rs7589998(A;A)
Make rs7589998(A;G)
Make rs7589998(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position60696885
is asnp
is mentioned by
dbSNPrs7589998
dbSNP (classic)rs7589998
ClinGenrs7589998
ebirs7589998
HLIrs7589998
Exacrs7589998
Gnomadrs7589998
Varsomers7589998
LitVarrs7589998
Maprs7589998
PheGenIrs7589998
Biobankrs7589998
1000 genomesrs7589998
hgdprs7589998
ensemblrs7589998
geneviewrs7589998
scholarrs7589998
googlers7589998
pharmgkbrs7589998
gwascentralrs7589998
openSNPrs7589998
23andMers7589998
SNPshotrs7589998
SNPdbers7589998
MSV3drs7589998
GWAS Ctlgrs7589998
GMAF0.04454
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 5E-6
Odds Ratio .03 [NR] g/d increase