Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Eurofins Ntd Llc |
RCV000180080 | SCV000232447 | uncertain significance | not provided | 2014-10-13 | criteria provided, single submitter | clinical testing | |
Labcorp Genetics |
RCV000180080 | SCV002276304 | likely benign | not provided | 2023-12-09 | criteria provided, single submitter | clinical testing | |
Gene |
RCV000180080 | SCV005628764 | uncertain significance | not provided | 2024-07-16 | criteria provided, single submitter | clinical testing | In silico analysis supports that this missense variant has a deleterious effect on protein structure/function; Has not been previously published as pathogenic or benign to our knowledge |