Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Counsyl | RCV000662550 | SCV000785133 | likely benign | Multiple endocrine neoplasia, type 1 | 2017-05-03 | criteria provided, single submitter | clinical testing | |
Labcorp Genetics |
RCV000662550 | SCV002392950 | likely benign | Multiple endocrine neoplasia, type 1 | 2024-09-02 | criteria provided, single submitter | clinical testing | |
Myriad Genetics, |
RCV000662550 | SCV004018044 | likely benign | Multiple endocrine neoplasia, type 1 | 2023-04-17 | criteria provided, single submitter | clinical testing | This variant is considered likely benign. This variant is intronic and is not expected to impact mRNA splicing. |