rs16966122
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs16966122(A;A) |
| Make rs16966122(A;G) |
| Make rs16966122(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 19 |
| Position | 31667558 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs16966122 |
| dbSNP (classic) | rs16966122 |
| ClinGen | rs16966122 |
| ebi | rs16966122 |
| HLI | rs16966122 |
| Exac | rs16966122 |
| Gnomad | rs16966122 |
| Varsome | rs16966122 |
| LitVar | rs16966122 |
| Map | rs16966122 |
| PheGenI | rs16966122 |
| Biobank | rs16966122 |
| 1000 genomes | rs16966122 |
| hgdp | rs16966122 |
| ensembl | rs16966122 |
| geneview | rs16966122 |
| scholar | rs16966122 |
| rs16966122 | |
| pharmgkb | rs16966122 |
| gwascentral | rs16966122 |
| openSNP | rs16966122 |
| 23andMe | rs16966122 |
| SNPshot | rs16966122 |
| SNPdbe | rs16966122 |
| MSV3d | rs16966122 |
| GWAS Ctlg | rs16966122 |
| GMAF | 0.1198 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23496005] |
| Trait | Narcolepsy with cataplexy |
| Title | Clinical, polysomnographic and genome-wide association analyses of narcolepsy with cataplexy: a European Narcolepsy Network study. |
| Risk Allele | |
| P-val | 2E-6 |
| Odds Ratio | 1.60 [NR] unit decrease |
