Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000867803 | SCV001009066 | likely benign | CHARGE association | 2024-01-26 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001712815 | SCV001942335 | likely benign | not provided | 2021-02-24 | criteria provided, single submitter | clinical testing | This variant is associated with the following publications: (PMID: 27899157, 28209183, 24819706) |