rs60794845
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;C) | 6.5 | Myofibrillar Myopathy |
| (C;C) | 0 | common in clinvar |
| Make rs60794845(C;T) |
| Make rs60794845(T;T) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 2 |
| Position | 219418599 |
| Gene | DES |
| is a | snp |
| is | mentioned by |
| dbSNP | rs60794845 |
| dbSNP (classic) | rs60794845 |
| ClinGen | rs60794845 |
| ebi | rs60794845 |
| HLI | rs60794845 |
| Exac | rs60794845 |
| Gnomad | rs60794845 |
| Varsome | rs60794845 |
| LitVar | rs60794845 |
| Map | rs60794845 |
| PheGenI | rs60794845 |
| Biobank | rs60794845 |
| 1000 genomes | rs60794845 |
| hgdp | rs60794845 |
| ensembl | rs60794845 |
| geneview | rs60794845 |
| scholar | rs60794845 |
| rs60794845 | |
| pharmgkb | rs60794845 |
| gwascentral | rs60794845 |
| openSNP | rs60794845 |
| 23andMe | rs60794845 |
| SNPshot | rs60794845 |
| SNPdbe | rs60794845 |
| MSV3d | rs60794845 |
| GWAS Ctlg | rs60794845 |
| Max Magnitude | 6.5 |
| ClinVar | |
|---|---|
| Risk | rs60794845(A;A) rs60794845(T;T) |
| Alt | rs60794845(A;A) rs60794845(T;T) |
| Reference | Rs60794845(C;C) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | DES |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000002.11:g.220283321C>A; NC_000002.11:g.220283321C>T |
| CLNSRC | UniProtKB (protein) |
| CLNACC | RCV000056793.1, RCV000056794.1, |
