Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Prevention |
RCV000247015 | SCV000312530 | benign | not specified | criteria provided, single submitter | clinical testing | ||
Gene |
RCV001660327 | SCV001873457 | benign | not provided | 2020-03-09 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV001808711 | SCV002057477 | benign | Arrhinia with choanal atresia and microphthalmia syndrome | 2021-07-15 | criteria provided, single submitter | clinical testing | |
Invitae | RCV002058261 | SCV002324478 | benign | Facioscapulohumeral muscular dystrophy 2 | 2024-02-01 | criteria provided, single submitter | clinical testing |