Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Eurofins Ntd Llc |
RCV000591676 | SCV000708977 | uncertain significance | not provided | 2018-06-21 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV000764872 | SCV000896028 | uncertain significance | Coffin-Lowry syndrome; Intellectual disability, X-linked 19 | 2021-11-30 | criteria provided, single submitter | clinical testing | |
Gene |
RCV000591676 | SCV002032463 | uncertain significance | not provided | 2021-12-07 | criteria provided, single submitter | clinical testing | In silico analysis supports that this missense variant does not alter protein structure/function; Has not been previously published as pathogenic or benign to our knowledge |