Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000440662 | SCV000533929 | likely benign | not provided | 2021-09-28 | criteria provided, single submitter | clinical testing | |
Invitae | RCV000533381 | SCV000654369 | benign | Left ventricular noncompaction 8 | 2024-01-19 | criteria provided, single submitter | clinical testing | |
Women's Health and Genetics/Laboratory Corporation of America, |
RCV003330680 | SCV004038554 | benign | not specified | 2023-08-19 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003942449 | SCV004756883 | likely benign | PRDM16-related condition | 2022-06-15 | 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). |