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rs6774852

From SNPedia

Orientationplus
Stabilizedplus
Make rs6774852(C;C)
Make rs6774852(C;T)
Make rs6774852(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position196351556
GeneUBXN7
is asnp
is mentioned by
dbSNPrs6774852
ebirs6774852
HLIrs6774852
Exacrs6774852
Varsomers6774852
Maprs6774852
PheGenIrs6774852
hapmaprs6774852
1000 genomesrs6774852
hgdprs6774852
ensemblrs6774852
gopubmedrs6774852
geneviewrs6774852
scholarrs6774852
googlers6774852
pharmgkbrs6774852
gwascentralrs6774852
openSNPrs6774852
23andMers6774852
23andMe allrs6774852
SNP Nexus

SNPshotrs6774852
SNPdbers6774852
MSV3drs6774852
GWAS Ctlgrs6774852
GMAF0.08861
Max Magnitude
? (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 7E-6
Odds Ratio .03 [NR] SD increase