Total submissions: 5
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Prevention |
RCV000252867 | SCV000315095 | benign | not specified | criteria provided, single submitter | clinical testing | ||
Gene |
RCV001722344 | SCV001946853 | benign | not provided | 2018-06-26 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV001815278 | SCV002062123 | benign | Arthrogryposis multiplex congenita 3, myogenic type | 2021-07-15 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV001815277 | SCV002062124 | benign | Emery-Dreifuss muscular dystrophy 4, autosomal dominant | 2021-07-15 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV001815276 | SCV002062125 | benign | Autosomal recessive ataxia, Beauce type | 2021-07-15 | criteria provided, single submitter | clinical testing |