Lynch Syndrome HNPCC Syndrome
| TEST CODE | MG00310 |
| TEST NAME | Lynch Syndrome HNPCC Syndrome |
| RELATED GENE | MSH2 |
| SYNONYMOUS | MSH2 |
| OMIM | 120435 |
| HEREDITY | Autosomal Dominant |
| CLINICAL AREA | Lynch Syndrome HNPCC Syndrome is an autosomal dominantly inherited disease. Mutations in the MSH2 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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