Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV002233446 | SCV000836291 | benign | Heterotopia, periventricular, X-linked dominant; Melnick-Needles syndrome; Oto-palato-digital syndrome, type II; Frontometaphyseal dysplasia | 2023-07-07 | criteria provided, single submitter | clinical testing | |
Diagnostic Laboratory, |
RCV001260710 | SCV001437802 | uncertain significance | Intellectual disability | 2020-09-10 | criteria provided, single submitter | clinical testing |