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rs16966389

From SNPedia

Orientationplus
Stabilizedplus
Make rs16966389(A;A)
Make rs16966389(A;G)
Make rs16966389(G;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position38172673
is asnp
is mentioned by
dbSNPrs16966389
ebirs16966389
HLIrs16966389
Exacrs16966389
Varsomers16966389
Maprs16966389
PheGenIrs16966389
hapmaprs16966389
1000 genomesrs16966389
hgdprs16966389
ensemblrs16966389
gopubmedrs16966389
geneviewrs16966389
scholarrs16966389
googlers16966389
pharmgkbrs16966389
gwascentralrs16966389
openSNPrs16966389
23andMers16966389
23andMe allrs16966389
SNP Nexus

SNPshotrs16966389
SNPdbers16966389
MSV3drs16966389
GWAS Ctlgrs16966389
GMAF0.1208
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23646285OA-icon.png]
Trait Hypersomnia (HLA-DQB1*06:02 negative)
Title Genome-wide association study of HLA-DQB1*06:02 negative essential hypersomnia.
Risk Allele G
P-val 7E-7
Odds Ratio 2.73 [1.82-4.10]