Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV001637871 | SCV001848772 | benign | not provided | 2018-08-07 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV001788664 | SCV002029574 | benign | Peroxisome biogenesis disorder 13A (Zellweger) | 2021-09-05 | criteria provided, single submitter | clinical testing |