Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Ambry Genetics | RCV000622630 | SCV000741372 | uncertain significance | Inborn genetic diseases | 2016-03-22 | criteria provided, single submitter | clinical testing | Lines of evidence used in support of classification: UNCERTAIN: Alteration(s) of Uncertain Clinical Significance Detected |
Invitae | RCV002532830 | SCV003009217 | likely benign | Charcot-Marie-Tooth disease axonal type 2O | 2022-05-21 | criteria provided, single submitter | clinical testing |