Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001482711 | SCV001687085 | likely benign | Heterotopia, periventricular, X-linked dominant; Melnick-Needles syndrome; Oto-palato-digital syndrome, type II; Frontometaphyseal dysplasia | 2023-10-10 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001551911 | SCV001772514 | likely benign | not provided | 2019-06-17 | criteria provided, single submitter | clinical testing |