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rs1476442

From SNPedia

Orientationplus
Stabilizedplus
Make rs1476442(A;A)
Make rs1476442(A;C)
Make rs1476442(C;C)
ReferenceGRCh38 38.1/142
Chromosome7
Position91643029
is asnp
is mentioned by
dbSNPrs1476442
ebirs1476442
HLIrs1476442
Exacrs1476442
Varsomers1476442
Maprs1476442
PheGenIrs1476442
hapmaprs1476442
1000 genomesrs1476442
hgdprs1476442
ensemblrs1476442
gopubmedrs1476442
geneviewrs1476442
scholarrs1476442
googlers1476442
pharmgkbrs1476442
gwascentralrs1476442
openSNPrs1476442
23andMers1476442
23andMe allrs1476442
SNP Nexus

SNPshotrs1476442
SNPdbers1476442
MSV3drs1476442
GWAS Ctlgrs1476442
Max Magnitude
? (A;A) (A;C) (C;C) 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 C
P-val 3E-6
Odds Ratio .02 [NR] mg/dL increase