rs8057394
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs8057394(C;C) |
| Make rs8057394(C;G) |
| Make rs8057394(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 10021631 |
| Gene | GRIN2A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs8057394 |
| dbSNP (classic) | rs8057394 |
| ClinGen | rs8057394 |
| ebi | rs8057394 |
| HLI | rs8057394 |
| Exac | rs8057394 |
| Gnomad | rs8057394 |
| Varsome | rs8057394 |
| LitVar | rs8057394 |
| Map | rs8057394 |
| PheGenI | rs8057394 |
| Biobank | rs8057394 |
| 1000 genomes | rs8057394 |
| hgdp | rs8057394 |
| ensembl | rs8057394 |
| geneview | rs8057394 |
| scholar | rs8057394 |
| rs8057394 | |
| pharmgkb | rs8057394 |
| gwascentral | rs8057394 |
| openSNP | rs8057394 |
| 23andMe | rs8057394 |
| SNPshot | rs8057394 |
| SNPdbe | rs8057394 |
| MSV3d | rs8057394 |
| GWAS Ctlg | rs8057394 |
| GMAF | 0.41 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 17569088] NR2A and NR2B receptor gene variations modify age at onset in Huntington disease in a sex-specific manner.
