Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000891663 | SCV001035489 | benign | Idiopathic generalized epilepsy; Hyperaldosteronism, familial, type IV | 2024-01-25 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003940693 | SCV004759528 | likely benign | CACNA1H-related condition | 2021-11-19 | criteria provided, single submitter | clinical testing | This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications). |