Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000899075 | SCV001043323 | likely benign | not provided | 2019-12-31 | criteria provided, single submitter | clinical testing | |
Centre for Mendelian Genomics, |
RCV001262774 | SCV001367432 | uncertain significance | Pigmented nodular adrenocortical disease, primary, 2 | 2019-04-05 | criteria provided, single submitter | clinical testing | This variant was classified as: Uncertain significance. The available evidence on this variant's pathogenicity is insufficient or conflicting. The following ACMG criteria were applied in classifying this variant: PVS1. |
Institute of Human Genetics, |
RCV001262774 | SCV001440765 | uncertain significance | Pigmented nodular adrenocortical disease, primary, 2 | 2019-01-01 | criteria provided, single submitter | clinical testing |