Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
International Society for Gastrointestinal Hereditary Tumours |
RCV000075590 | SCV000106587 | uncertain significance | Lynch syndrome | 2019-06-21 | reviewed by expert panel | curation | Insufficient evidence: extends protein by 25 amino acids |
Mendelics | RCV000075590 | SCV000838031 | likely pathogenic | Lynch syndrome | 2018-07-02 | criteria provided, single submitter | clinical testing |