rs220599
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs220599(A;A) |
| Make rs220599(A;G) |
| Make rs220599(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 13822364 |
| Gene | GRIN2B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs220599 |
| dbSNP (classic) | rs220599 |
| ClinGen | rs220599 |
| ebi | rs220599 |
| HLI | rs220599 |
| Exac | rs220599 |
| Gnomad | rs220599 |
| Varsome | rs220599 |
| LitVar | rs220599 |
| Map | rs220599 |
| PheGenI | rs220599 |
| Biobank | rs220599 |
| 1000 genomes | rs220599 |
| hgdp | rs220599 |
| ensembl | rs220599 |
| geneview | rs220599 |
| scholar | rs220599 |
| rs220599 | |
| pharmgkb | rs220599 |
| gwascentral | rs220599 |
| openSNP | rs220599 |
| 23andMe | rs220599 |
| SNPshot | rs220599 |
| SNPdbe | rs220599 |
| MSV3d | rs220599 |
| GWAS Ctlg | rs220599 |
| GMAF | 0.4628 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 21281445] Polymorphisms associated with normal memory variation also affect memory impairment in schizophrenia
