rs139969658
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs139969658(C;T) |
| Make rs139969658(T;T) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 6 |
| Position | 7585738 |
| Gene | DSP |
| is a | snp |
| is | mentioned by |
| dbSNP | rs139969658 |
| dbSNP (classic) | rs139969658 |
| ClinGen | rs139969658 |
| ebi | rs139969658 |
| HLI | rs139969658 |
| Exac | rs139969658 |
| Gnomad | rs139969658 |
| Varsome | rs139969658 |
| LitVar | rs139969658 |
| Map | rs139969658 |
| PheGenI | rs139969658 |
| Biobank | rs139969658 |
| 1000 genomes | rs139969658 |
| hgdp | rs139969658 |
| ensembl | rs139969658 |
| geneview | rs139969658 |
| scholar | rs139969658 |
| rs139969658 | |
| pharmgkb | rs139969658 |
| gwascentral | rs139969658 |
| openSNP | rs139969658 |
| 23andMe | rs139969658 |
| SNPshot | rs139969658 |
| SNPdbe | rs139969658 |
| MSV3d | rs139969658 |
| GWAS Ctlg | rs139969658 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs139969658(T;T) |
| Alt | rs139969658(T;T) |
| Reference | Rs139969658(C;C) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | DSP |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000006.11:g.7585971C>T |
| CLNSRC | |
| CLNACC | RCV000181351.2, |
