Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001424328 | SCV001626924 | likely benign | Heterotopia, periventricular, X-linked dominant; Melnick-Needles syndrome; Oto-palato-digital syndrome, type II; Frontometaphyseal dysplasia | 2022-03-19 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001552421 | SCV001773104 | likely benign | not provided | 2020-05-29 | criteria provided, single submitter | clinical testing |