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rs2065779

From SNPedia

Orientationplus
Stabilizedplus
Make rs2065779(C;C)
Make rs2065779(C;G)
Make rs2065779(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position111118043
is asnp
is mentioned by
dbSNPrs2065779
ebirs2065779
HLIrs2065779
Exacrs2065779
Varsomers2065779
Maprs2065779
PheGenIrs2065779
hapmaprs2065779
1000 genomesrs2065779
hgdprs2065779
ensemblrs2065779
gopubmedrs2065779
geneviewrs2065779
scholarrs2065779
googlers2065779
pharmgkbrs2065779
gwascentralrs2065779
openSNPrs2065779
23andMers2065779
23andMe allrs2065779
SNP Nexus

SNPshotrs2065779
SNPdbers2065779
MSV3drs2065779
GWAS Ctlgrs2065779
GMAF0.2911
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 22754043OA-icon.png]
Trait Insomnia (caffeine-induced)
Title A genome-wide association study of caffeine-related sleep disturbance: confirmation of a role for a common variant in the adenosine receptor.
Risk Allele
P-val 3E-6
Odds Ratio 1.82 [1.41-2.33]