Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Ambry Genetics | RCV000129879 | SCV000184696 | uncertain significance | Hereditary cancer-predisposing syndrome | 2014-03-05 | criteria provided, single submitter | clinical testing | |
Gene |
RCV002051812 | SCV002319137 | uncertain significance | not provided | 2023-09-11 | criteria provided, single submitter | clinical testing | Has not been previously published as pathogenic or benign to our knowledge; No data available from control populations to assess the frequency of this variant; Also known as c.-862G>T |