Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV003830844 | SCV004635251 | likely benign | Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency | 2022-11-15 | criteria provided, single submitter | clinical testing |