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rs16872248

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common genotype
Make rs16872248(C;T)
Make rs16872248(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position22019877
is asnp
is mentioned by
dbSNPrs16872248
dbSNP (classic)rs16872248
ClinGenrs16872248
ebirs16872248
HLIrs16872248
Exacrs16872248
Gnomadrs16872248
Varsomers16872248
LitVarrs16872248
Maprs16872248
PheGenIrs16872248
Biobankrs16872248
1000 genomesrs16872248
hgdprs16872248
ensemblrs16872248
geneviewrs16872248
scholarrs16872248
googlers16872248
pharmgkbrs16872248
gwascentralrs16872248
openSNPrs16872248
23andMers16872248
SNPshotrs16872248
SNPdbers16872248
MSV3drs16872248
GWAS Ctlgrs16872248
GMAF0.1028
Max Magnitude0
? (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 6E-6
Odds Ratio .03 [NR] % increase