Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000952555 | SCV001099070 | likely benign | not provided | 2018-12-19 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003935797 | SCV004755366 | likely benign | PLAT-related condition | 2022-02-15 | 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). |