rs751181600
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs751181600(G;T) |
| Make rs751181600(T;T) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 16 |
| Position | 78164284 |
| Gene | WWOX |
| is a | snp |
| is | mentioned by |
| dbSNP | rs751181600 |
| dbSNP (classic) | rs751181600 |
| ClinGen | rs751181600 |
| ebi | rs751181600 |
| HLI | rs751181600 |
| Exac | rs751181600 |
| Gnomad | rs751181600 |
| Varsome | rs751181600 |
| LitVar | rs751181600 |
| Map | rs751181600 |
| PheGenI | rs751181600 |
| Biobank | rs751181600 |
| 1000 genomes | rs751181600 |
| hgdp | rs751181600 |
| ensembl | rs751181600 |
| geneview | rs751181600 |
| scholar | rs751181600 |
| rs751181600 | |
| pharmgkb | rs751181600 |
| gwascentral | rs751181600 |
| openSNP | rs751181600 |
| 23andMe | rs751181600 |
| SNPshot | rs751181600 |
| SNPdbe | rs751181600 |
| MSV3d | rs751181600 |
| GWAS Ctlg | rs751181600 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs751181600(T;T) |
| Alt | rs751181600(T;T) |
| Reference | Rs751181600(G;G) |
| Significance | Probable-Pathogenic |
| Disease | Spinocerebellar ataxia |
| Variation | info |
| Gene | WWOX |
| CLNDBN | Spinocerebellar ataxia, autosomal recessive 12 |
| Reversed | 0 |
| HGVS | NC_000016.9:g.78198181G>T |
| CLNSRC | |
| CLNACC | RCV000490293.1, |
