Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001235256 | SCV001407935 | benign | Heterotopia, periventricular, X-linked dominant; Melnick-Needles syndrome; Oto-palato-digital syndrome, type II; Frontometaphyseal dysplasia | 2023-11-17 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001732085 | SCV001982506 | likely benign | not provided | 2021-03-30 | criteria provided, single submitter | clinical testing |