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rs1549059

From SNPedia

Orientationplus
Stabilizedplus
Make rs1549059(C;C)
Make rs1549059(C;T)
Make rs1549059(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position105596960
is asnp
is mentioned by
dbSNPrs1549059
ebirs1549059
HLIrs1549059
Exacrs1549059
Varsomers1549059
Maprs1549059
PheGenIrs1549059
hapmaprs1549059
1000 genomesrs1549059
hgdprs1549059
ensemblrs1549059
gopubmedrs1549059
geneviewrs1549059
scholarrs1549059
googlers1549059
pharmgkbrs1549059
gwascentralrs1549059
openSNPrs1549059
23andMers1549059
23andMe allrs1549059
SNP Nexus

SNPshotrs1549059
SNPdbers1549059
MSV3drs1549059
GWAS Ctlgrs1549059
GMAF0.4284
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 4E-6
Odds Ratio .03 [NR] kcal/d increase