Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000861073 | SCV000719032 | likely benign | not provided | 2020-03-06 | criteria provided, single submitter | clinical testing | |
Invitae | RCV001471848 | SCV001675964 | likely benign | Heterotopia, periventricular, X-linked dominant; Melnick-Needles syndrome; Oto-palato-digital syndrome, type II; Frontometaphyseal dysplasia | 2022-09-27 | criteria provided, single submitter | clinical testing |