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rs16867321

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs16867321(C;T)
Make rs16867321(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position180497652
is asnp
is mentioned by
dbSNPrs16867321
ebirs16867321
HLIrs16867321
Exacrs16867321
Varsomers16867321
Maprs16867321
PheGenIrs16867321
hapmaprs16867321
1000 genomesrs16867321
hgdprs16867321
ensemblrs16867321
gopubmedrs16867321
geneviewrs16867321
scholarrs16867321
googlers16867321
pharmgkbrs16867321
gwascentralrs16867321
openSNPrs16867321
23andMers16867321
23andMe allrs16867321
SNP Nexus

SNPshotrs16867321
SNPdbers16867321
MSV3drs16867321
GWAS Ctlgrs16867321
GMAF0.2713
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21552555OA-icon.png]
Trait
Title A genome-wide association study on obesity and obesity-related traits.
Risk Allele
P-val 0.000002
Odds Ratio None None