Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Laboratory for Molecular Medicine, |
RCV000454552 | SCV000538808 | benign | not specified | 2016-03-29 | criteria provided, single submitter | clinical testing | Variant identified in a genome or exome case(s) and assessed due to predicted null impact of the variant or pathogenic assertions in the literature or databases. Disclaimer: This variant has not undergone full assessment. The following are preliminary notes: Frequency |
Invitae | RCV001515946 | SCV001724133 | benign | Spermatogenic failure 18; Ciliary dyskinesia, primary, 37 | 2024-01-31 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001653786 | SCV001866413 | benign | not provided | 2018-07-05 | criteria provided, single submitter | clinical testing |