Yes
| Variant Name | Allele Count | Allele Frequency | Associated Disease | Associated Gene |
|---|---|---|---|---|
| NM_000053.3:c.1216T>G | ||||
| NM_000053.3:c.2495A>G | ||||
| NM_000053.3:c.3419T>C | ||||
| NM_000053.3:c.2855G>A | ||||
| NM_000053.3:c.2866-2A>G | 2 | |||
| NM_000053.3:c.1366G>C | ||||
| NM_000053.3:c.1544-53A>C | ||||
| NM_000053.3:c.2448-25G>A | ||||
| NM_000053.3:c.2866-90G>T | ||||
| NM_000053.3:c.3045G>A | ||||
| NM_000053.3:c.3903+6C>T |