rs61726467
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs61726467(A;A) |
| Make rs61726467(A;G) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 2 |
| Position | 219421553 |
| Gene | DES |
| is a | snp |
| is | mentioned by |
| dbSNP | rs61726467 |
| dbSNP (classic) | rs61726467 |
| ClinGen | rs61726467 |
| ebi | rs61726467 |
| HLI | rs61726467 |
| Exac | rs61726467 |
| Gnomad | rs61726467 |
| Varsome | rs61726467 |
| LitVar | rs61726467 |
| Map | rs61726467 |
| PheGenI | rs61726467 |
| Biobank | rs61726467 |
| 1000 genomes | rs61726467 |
| hgdp | rs61726467 |
| ensembl | rs61726467 |
| geneview | rs61726467 |
| scholar | rs61726467 |
| rs61726467 | |
| pharmgkb | rs61726467 |
| gwascentral | rs61726467 |
| openSNP | rs61726467 |
| 23andMe | rs61726467 |
| SNPshot | rs61726467 |
| SNPdbe | rs61726467 |
| MSV3d | rs61726467 |
| GWAS Ctlg | rs61726467 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs61726467(A;A) |
| Alt | rs61726467(A;A) |
| Reference | Rs61726467(G;G) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | DES |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000002.11:g.220286275G>A |
| CLNSRC | |
| CLNACC | RCV000056782.3, |
