CWC27
From SNPedia
| is a | gene |
| is | mentioned by |
| ClinVar | CWC27 |
| GeneCards | CWC27 |
| Diseases | CWC27 |
| wikipedia | CWC27 |
| CWC27 | |
| gopubmed | CWC27 |
| EVS | CWC27 |
| HEFalMp | CWC27 |
| MyGene2 | CWC27 |
| 23andMe | CWC27 |
| # SNPs | 4 |
| Max Magnitude | Chromosome position | Summary | |
|---|---|---|---|
| rs1085307446 | 0 | 64,785,579 | |
| rs1085307447 | 0 | 64,885,447 | |
| rs1085307448 | 0 | 64,885,506 | |
| rs781702398 | 0 | 64,788,968 |
Mutations in the Spliceosome Component CWC27 Cause retinal degeneration with or without Additional Developmental Anomalies: 10.1016/j.ajhg.2017.02.008
Related press release
