rs771610568
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs771610568(C;C) |
| Make rs771610568(C;T) |
| Make rs771610568(T;T) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 9 |
| Position | 137162676 |
| Gene | GRIN1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs771610568 |
| dbSNP (classic) | rs771610568 |
| ClinGen | rs771610568 |
| ebi | rs771610568 |
| HLI | rs771610568 |
| Exac | rs771610568 |
| Gnomad | rs771610568 |
| Varsome | rs771610568 |
| LitVar | rs771610568 |
| Map | rs771610568 |
| PheGenI | rs771610568 |
| Biobank | rs771610568 |
| 1000 genomes | rs771610568 |
| hgdp | rs771610568 |
| ensembl | rs771610568 |
| geneview | rs771610568 |
| scholar | rs771610568 |
| rs771610568 | |
| pharmgkb | rs771610568 |
| gwascentral | rs771610568 |
| openSNP | rs771610568 |
| 23andMe | rs771610568 |
| SNPshot | rs771610568 |
| SNPdbe | rs771610568 |
| MSV3d | rs771610568 |
| GWAS Ctlg | rs771610568 |
| Max Magnitude | 0 |
aka NM_007327.3(GRIN1):c.1950C>G or (p.Asn650Lys)
OMIM pathogenic variant
