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rs4864548

From SNPedia

discrepancy in risk assignment
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) normal
(A;G) 1.8x higher risk for obesity if in haplotype
(G;G) 0 1.8x higher risk for obesity if in haplotype
ReferenceGRCh38 38.1/141
Chromosome4
Position55547636
GeneCLOCK
is asnp
is mentioned by
dbSNPrs4864548
ebirs4864548
HLIrs4864548
Exacrs4864548
Varsomers4864548
Maprs4864548
PheGenIrs4864548
hapmaprs4864548
1000 genomesrs4864548
hgdprs4864548
ensemblrs4864548
gopubmedrs4864548
geneviewrs4864548
scholarrs4864548
googlers4864548
pharmgkbrs4864548
gwascentralrs4864548
openSNPrs4864548
23andMers4864548
23andMe allrs4864548
SNP Nexus

SNPshotrs4864548
SNPdbers4864548
MSV3drs4864548
GWAS Ctlgrs4864548
GMAF0.3861
Max Magnitude0
? (A;A) (A;G) (G;G) 28
A study of 391 overweight patients concluded that the haplotype of rs1554483(G) and rs4864548(A) was associated with a 1.8-fold higher risk (CI: 1.31-2.54, p < 0.001) of obesity.[PMID 18541547]


[PMID 17696255OA-icon.png] Common genetic variations in CLOCK transcription factor are associated with nonalcoholic fatty liver disease.


[PMID 18071340] Association between polymorphisms in the Clock gene, obesity and the metabolic syndrome in man.