Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Eurofins Ntd Llc |
RCV000732227 | SCV000860150 | uncertain significance | not provided | 2018-03-13 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002485910 | SCV002780705 | uncertain significance | Autosomal recessive ataxia, Beauce type; Emery-Dreifuss muscular dystrophy 4, autosomal dominant; Arthrogryposis multiplex congenita 3, myogenic type | 2022-04-04 | criteria provided, single submitter | clinical testing |