Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Prevention |
RCV003983368 | SCV004800320 | uncertain significance | PKHD1-related disorder | 2024-01-29 | criteria provided, single submitter | clinical testing | The PKHD1 c.284C>T variant is predicted to result in the amino acid substitution p.Ser95Phe. To our knowledge, this variant has not been reported in the literature. This variant is reported in 0.00088% of alleles in individuals of European (Non-Finnish) descent in gnomAD. At this time, the clinical significance of this variant is uncertain due to the absence of conclusive functional and genetic evidence. |