Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV003501484 | SCV004277568 | likely benign | Ataxia-telangiectasia syndrome | 2023-10-06 | criteria provided, single submitter | clinical testing | |
Myriad Genetics, |
RCV004593328 | SCV005085471 | likely benign | Familial cancer of breast | 2024-06-24 | criteria provided, single submitter | clinical testing | This variant is considered likely benign. This variant is intronic and is not expected to impact mRNA splicing. |