Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Centre for Mendelian Genomics, |
RCV001248764 | SCV001366809 | uncertain significance | Polycystic kidney disease, adult type | 2019-08-19 | 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: PP3. |
Center For Human Genetics And Laboratory Diagnostics, |
RCV001248764 | SCV001422273 | uncertain significance | Polycystic kidney disease, adult type | 2019-10-23 | criteria provided, single submitter | clinical testing |