Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Molecular Genetics Laboratory, |
RCV001173537 | SCV001336627 | likely benign | Charcot-Marie-Tooth disease | criteria provided, single submitter | clinical testing | ||
Labcorp Genetics |
RCV001484651 | SCV001689071 | likely benign | Amyloidosis, hereditary systemic 1 | 2023-09-05 | criteria provided, single submitter | clinical testing |