rs372245668
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs372245668(C;T) |
| Make rs372245668(T;T) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 6 |
| Position | 24658560 |
| Gene | TDP2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs372245668 |
| dbSNP (classic) | rs372245668 |
| ClinGen | rs372245668 |
| ebi | rs372245668 |
| HLI | rs372245668 |
| Exac | rs372245668 |
| Gnomad | rs372245668 |
| Varsome | rs372245668 |
| LitVar | rs372245668 |
| Map | rs372245668 |
| PheGenI | rs372245668 |
| Biobank | rs372245668 |
| 1000 genomes | rs372245668 |
| hgdp | rs372245668 |
| ensembl | rs372245668 |
| geneview | rs372245668 |
| scholar | rs372245668 |
| rs372245668 | |
| pharmgkb | rs372245668 |
| gwascentral | rs372245668 |
| openSNP | rs372245668 |
| 23andMe | rs372245668 |
| SNPshot | rs372245668 |
| SNPdbe | rs372245668 |
| MSV3d | rs372245668 |
| GWAS Ctlg | rs372245668 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs372245668(T;T) |
| Alt | rs372245668(T;T) |
| Reference | Rs372245668(C;C) |
| Significance | Pathogenic |
| Disease | Spinocerebellar ataxia |
| Variation | info |
| Gene | TDP2 |
| CLNDBN | Spinocerebellar ataxia, autosomal recessive 23 |
| Reversed | 0 |
| HGVS | NC_000006.11:g.24658788C>T |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000211705.1, |
