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rs8066099

From SNPedia

Orientationplus
Stabilizedplus
Make rs8066099(C;C)
Make rs8066099(C;T)
Make rs8066099(T;T)
ReferenceGRCh38 38.1/142
Chromosome17
Position14986608
is asnp
is mentioned by
dbSNPrs8066099
ebirs8066099
HLIrs8066099
Exacrs8066099
Varsomers8066099
Maprs8066099
PheGenIrs8066099
hapmaprs8066099
1000 genomesrs8066099
hgdprs8066099
ensemblrs8066099
gopubmedrs8066099
geneviewrs8066099
scholarrs8066099
googlers8066099
pharmgkbrs8066099
gwascentralrs8066099
openSNPrs8066099
23andMers8066099
23andMe allrs8066099
SNP Nexus

SNPshotrs8066099
SNPdbers8066099
MSV3drs8066099
GWAS Ctlgrs8066099
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 A
P-val 2E-6
Odds Ratio .03 [NR] pg/mL increase