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rs16905439

From SNPedia

Orientationplus
Stabilizedplus
Make rs16905439(C;C)
Make rs16905439(C;T)
Make rs16905439(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position135976961
is asnp
is mentioned by
dbSNPrs16905439
dbSNP (old)rs16905439
ClinGenrs16905439
ebirs16905439
HLIrs16905439
Exacrs16905439
Varsomers16905439
Maprs16905439
PheGenIrs16905439
Biobankrs16905439
1000 genomesrs16905439
hgdprs16905439
ensemblrs16905439
gopubmedrs16905439
geneviewrs16905439
scholarrs16905439
googlers16905439
pharmgkbrs16905439
gwascentralrs16905439
openSNPrs16905439
23andMers16905439
23andMe allrs16905439
SNP Nexus

SNPshotrs16905439
SNPdbers16905439
MSV3drs16905439
GWAS Ctlgrs16905439
GMAF0.1047
Max Magnitude
? (C;C) (C;T) (T;T) 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 9E-6
Odds Ratio 3.33 [1.96-5.88]