Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Biologie des Tumeurs Solides, |
RCV000754776 | SCV000864261 | pathogenic | Lynch syndrome 1 | 2018-05-23 | criteria provided, single submitter | clinical testing | This variant was identified in 3 DNA samples from patients with Lynch syndrome in the same family. It was not detected in an unaffected member's DNA sample from the same family. |