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rs996712

From SNPedia

Orientationminus
Stabilizedminus
Make rs996712(C;C)
Make rs996712(C;T)
Make rs996712(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position53275637
is asnp
is mentioned by
dbSNPrs996712
ebirs996712
HLIrs996712
Exacrs996712
Varsomers996712
Maprs996712
PheGenIrs996712
hapmaprs996712
1000 genomesrs996712
hgdprs996712
ensemblrs996712
gopubmedrs996712
geneviewrs996712
scholarrs996712
googlers996712
pharmgkbrs996712
gwascentralrs996712
openSNPrs996712
23andMers996712
23andMe allrs996712
SNP Nexus

SNPshotrs996712
SNPdbers996712
MSV3drs996712
GWAS Ctlgrs996712
GMAF0.3095
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 8E-6
Odds Ratio .02 [NR] pg/mL increase