Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Hudson |
RCV000761589 | SCV000891748 | uncertain significance | Congenital myopathy 4B, autosomal recessive | 2018-04-18 | criteria provided, single submitter | research | ACMG codes: PM2, PP3 |