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rs16923476

From SNPedia

Orientationplus
Stabilizedplus
Make rs16923476(A;A)
Make rs16923476(A;G)
Make rs16923476(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position23569282
is asnp
is mentioned by
dbSNPrs16923476
ebirs16923476
HLIrs16923476
Exacrs16923476
Varsomers16923476
Maprs16923476
PheGenIrs16923476
hapmaprs16923476
1000 genomesrs16923476
hgdprs16923476
ensemblrs16923476
gopubmedrs16923476
geneviewrs16923476
scholarrs16923476
googlers16923476
pharmgkbrs16923476
gwascentralrs16923476
openSNPrs16923476
23andMers16923476
23andMe allrs16923476
SNP Nexus

SNPshotrs16923476
SNPdbers16923476
MSV3drs16923476
GWAS Ctlgrs16923476
GMAF0.08724
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23563609OA-icon.png]
Trait Obesity (early onset extreme)
Title Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity.
Risk Allele A
P-val 1E-7
Odds Ratio 1.78 [1.44-2.20]