Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
ARUP Laboratories, |
RCV001810702 | SCV001477856 | likely benign | not provided | 2019-10-29 | criteria provided, single submitter | clinical testing | |
Invitae | RCV001810702 | SCV002339565 | likely benign | not provided | 2023-05-18 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV003127759 | SCV003801588 | likely benign | Seckel syndrome 1 | 2023-02-08 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV003127760 | SCV003801589 | likely benign | Familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome | 2023-02-08 | criteria provided, single submitter | clinical testing |