Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Revvity Omics, |
RCV003144010 | SCV003832735 | uncertain significance | not provided | 2019-07-17 | criteria provided, single submitter | clinical testing | |
Labcorp Genetics |
RCV003778874 | SCV004569575 | benign | Heterotopia, periventricular, X-linked dominant; Melnick-Needles syndrome; Oto-palato-digital syndrome, type II; Frontometaphyseal dysplasia | 2023-07-08 | criteria provided, single submitter | clinical testing |