Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000952386 | SCV000722709 | likely benign | not provided | 2021-05-28 | criteria provided, single submitter | clinical testing | |
Invitae | RCV001496220 | SCV001700914 | likely benign | Heterotopia, periventricular, X-linked dominant; Melnick-Needles syndrome; Oto-palato-digital syndrome, type II; Frontometaphyseal dysplasia | 2023-04-28 | criteria provided, single submitter | clinical testing |