rs990150249
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 16 |
| Position | 78115000 |
| Gene | WWOX |
| is a | snp |
| is | mentioned by |
| dbSNP | rs990150249 |
| dbSNP (classic) | rs990150249 |
| ClinGen | rs990150249 |
| ebi | rs990150249 |
| HLI | rs990150249 |
| Exac | rs990150249 |
| Gnomad | rs990150249 |
| Varsome | rs990150249 |
| LitVar | rs990150249 |
| Map | rs990150249 |
| PheGenI | rs990150249 |
| Biobank | rs990150249 |
| 1000 genomes | rs990150249 |
| hgdp | rs990150249 |
| ensembl | rs990150249 |
| geneview | rs990150249 |
| scholar | rs990150249 |
| rs990150249 | |
| pharmgkb | rs990150249 |
| gwascentral | rs990150249 |
| openSNP | rs990150249 |
| 23andMe | rs990150249 |
| SNPshot | rs990150249 |
| SNPdbe | rs990150249 |
| MSV3d | rs990150249 |
| GWAS Ctlg | rs990150249 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs990150249(G;G) |
| Alt | rs990150249(G;G) |
| Reference | Rs990150249(C;C) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000016.9:g.78148897C>G |
| CLNSRC | |
| CLNACC | RCV000487411.1, |
