rs9390754
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs9390754(A;A) |
| Make rs9390754(A;G) |
| Make rs9390754(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 101517038 |
| Gene | GRIK2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9390754 |
| dbSNP (classic) | rs9390754 |
| ClinGen | rs9390754 |
| ebi | rs9390754 |
| HLI | rs9390754 |
| Exac | rs9390754 |
| Gnomad | rs9390754 |
| Varsome | rs9390754 |
| LitVar | rs9390754 |
| Map | rs9390754 |
| PheGenI | rs9390754 |
| Biobank | rs9390754 |
| 1000 genomes | rs9390754 |
| hgdp | rs9390754 |
| ensembl | rs9390754 |
| geneview | rs9390754 |
| scholar | rs9390754 |
| rs9390754 | |
| pharmgkb | rs9390754 |
| gwascentral | rs9390754 |
| openSNP | rs9390754 |
| 23andMe | rs9390754 |
| SNPshot | rs9390754 |
| SNPdbe | rs9390754 |
| MSV3d | rs9390754 |
| GWAS Ctlg | rs9390754 |
| GMAF | 0.2663 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 22116939] Two-stage genome-wide association study identifies variants in CAMSAP1L1 as susceptibility loci for epilepsy in Chinese
[PMID 27324535
] [Association between glutamate receptor 2 polymorphisms and epilepsy in children].
