Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Mendelics | RCV000709518 | SCV000839342 | likely pathogenic | Hereditary breast ovarian cancer syndrome | 2018-07-02 | criteria provided, single submitter | clinical testing | |
Mendelics | RCV000989966 | SCV001140728 | likely pathogenic | Fanconi anemia complementation group O | 2019-05-28 | criteria provided, single submitter | clinical testing |