Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
International Society for Gastrointestinal Hereditary Tumours |
RCV000782001 | SCV000920461 | uncertain significance | Lynch syndrome | 2018-12-19 | reviewed by expert panel | curation | Conflicting information: In Parc et al (PMID: 12624141) it is reported as de novo in supplementary, but on UMD it is classified as likely neutral. |