rs747838255
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs747838255(A;A) |
| Make rs747838255(A;G) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 16 |
| Position | 9840746 |
| Gene | GRIN2A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs747838255 |
| dbSNP (classic) | rs747838255 |
| ClinGen | rs747838255 |
| ebi | rs747838255 |
| HLI | rs747838255 |
| Exac | rs747838255 |
| Gnomad | rs747838255 |
| Varsome | rs747838255 |
| LitVar | rs747838255 |
| Map | rs747838255 |
| PheGenI | rs747838255 |
| Biobank | rs747838255 |
| 1000 genomes | rs747838255 |
| hgdp | rs747838255 |
| ensembl | rs747838255 |
| geneview | rs747838255 |
| scholar | rs747838255 |
| rs747838255 | |
| pharmgkb | rs747838255 |
| gwascentral | rs747838255 |
| openSNP | rs747838255 |
| 23andMe | rs747838255 |
| SNPshot | rs747838255 |
| SNPdbe | rs747838255 |
| MSV3d | rs747838255 |
| GWAS Ctlg | rs747838255 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs747838255(A;A) |
| Alt | rs747838255(A;A) |
| Reference | Rs747838255(G;G) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | GRIN2A |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000016.9:g.9934603G>A |
| CLNSRC | |
| CLNACC | RCV000187674.2, |
