Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV000931073 | SCV001076736 | likely benign | Familial melanoma | 2025-01-06 | criteria provided, single submitter | clinical testing | |
Myriad Genetics, |
RCV004789258 | SCV005402766 | likely benign | Melanoma, cutaneous malignant, susceptibility to, 3 | 2024-09-25 | criteria provided, single submitter | clinical testing | This variant is considered likely benign. This variant is intronic and is not expected to impact mRNA splicing. |