Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV001638850 | SCV001852254 | benign | not provided | 2021-03-29 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV001810162 | SCV002057467 | benign | Arrhinia with choanal atresia and microphthalmia syndrome | 2021-07-15 | criteria provided, single submitter | clinical testing | |
Invitae | RCV002072956 | SCV002407176 | benign | Facioscapulohumeral muscular dystrophy 2 | 2024-01-31 | criteria provided, single submitter | clinical testing |