rs16826005
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs16826005(A;A) |
Make rs16826005(A;G) |
Make rs16826005(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 133508430 |
Gene | NCKAP5 |
is a | snp |
is | mentioned by |
dbSNP | rs16826005 |
dbSNP (classic) | rs16826005 |
ClinGen | rs16826005 |
ebi | rs16826005 |
HLI | rs16826005 |
Exac | rs16826005 |
Gnomad | rs16826005 |
Varsome | rs16826005 |
LitVar | rs16826005 |
Map | rs16826005 |
PheGenI | rs16826005 |
Biobank | rs16826005 |
1000 genomes | rs16826005 |
hgdp | rs16826005 |
ensembl | rs16826005 |
geneview | rs16826005 |
scholar | rs16826005 |
rs16826005 | |
pharmgkb | rs16826005 |
gwascentral | rs16826005 |
openSNP | rs16826005 |
23andMe | rs16826005 |
SNPshot | rs16826005 |
SNPdbe | rs16826005 |
MSV3d | rs16826005 |
GWAS Ctlg | rs16826005 |
GMAF | 0.1382 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23646285] |
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 | 1E-7 |
Odds Ratio | 3.52 [2.17-5.70] |