Short QT Syndrome 2
| TEST CODE | MG09960 |
| TEST NAME | Short QT Syndrome 2 |
| RELATED GENE | KCNQ1 |
| SYNONYMOUS | KCNQ1 |
| OMIM | 609621 |
| HEREDITY | Autosomal Dominant |
| CLINICAL AREA | Short QT Syndrome 2 is an autosomal dominantly inherited disease. Mutations in the KCNQ1 gene have been associated with the disease. |
| METHOD | Next Generation Sequencing |
| SAMPLE TYPE | Blood with EDTA |
| QUANTITY | 3 mL |
| TAT | 40 DAYS |
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