Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Mendelics | RCV000987345 | SCV001136620 | benign | Seckel syndrome 1 | 2019-05-28 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001712835 | SCV001943591 | benign | not provided | 2019-08-10 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV000987345 | SCV003801815 | benign | Seckel syndrome 1 | 2023-02-08 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV003127561 | SCV003801817 | benign | Familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome | 2023-02-08 | criteria provided, single submitter | clinical testing |