rs9947662
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs9947662(A;A) |
| Make rs9947662(A;G) |
| Make rs9947662(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 18 |
| Position | 47333893 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9947662 |
| dbSNP (classic) | rs9947662 |
| ClinGen | rs9947662 |
| ebi | rs9947662 |
| HLI | rs9947662 |
| Exac | rs9947662 |
| Gnomad | rs9947662 |
| Varsome | rs9947662 |
| LitVar | rs9947662 |
| Map | rs9947662 |
| PheGenI | rs9947662 |
| Biobank | rs9947662 |
| 1000 genomes | rs9947662 |
| hgdp | rs9947662 |
| ensembl | rs9947662 |
| geneview | rs9947662 |
| scholar | rs9947662 |
| rs9947662 | |
| pharmgkb | rs9947662 |
| gwascentral | rs9947662 |
| openSNP | rs9947662 |
| 23andMe | rs9947662 |
| SNPshot | rs9947662 |
| SNPdbe | rs9947662 |
| MSV3d | rs9947662 |
| GWAS Ctlg | rs9947662 |
| GMAF | 0.2406 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23793025 ]
|
| Trait | Migraine |
| Title | Genome-wide meta-analysis identifies new susceptibility loci for migraine. |
| Risk Allele | |
| P-val | 3E-6 |
| Odds Ratio | 1.06 [1.03-1.09] |
