Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Ambry Genetics | RCV000571053 | SCV000662083 | uncertain significance | Hereditary cancer-predisposing syndrome | 2019-06-07 | criteria provided, single submitter | clinical testing | Insufficient evidence |
Color | RCV000571053 | SCV000908657 | uncertain significance | Hereditary cancer-predisposing syndrome | 2018-07-12 | criteria provided, single submitter | clinical testing |