Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV000583138 | SCV000691098 | likely benign | Hereditary cancer-predisposing syndrome | 2017-10-02 | criteria provided, single submitter | clinical testing | |
Sema4, |
RCV000583138 | SCV002530379 | uncertain significance | Hereditary cancer-predisposing syndrome | 2022-01-01 | criteria provided, single submitter | curation | |
KCCC/NGS Laboratory, |
RCV003316770 | SCV004016599 | likely benign | Lynch syndrome 4 | 2023-07-07 | criteria provided, single submitter | clinical testing |