Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000463160 | SCV000556062 | benign | Heterotopia, periventricular, X-linked dominant; Melnick-Needles syndrome; Oto-palato-digital syndrome, type II; Frontometaphyseal dysplasia | 2023-12-27 | criteria provided, single submitter | clinical testing | |
Genome Diagnostics Laboratory, |
RCV001580099 | SCV001809672 | likely benign | not provided | no assertion criteria provided | clinical testing | ||
Genome Diagnostics Laboratory, |
RCV001580099 | SCV001929752 | likely benign | not provided | no assertion criteria provided | clinical testing |