Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV003833992 | SCV004634732 | likely benign | Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency | 2023-11-07 | criteria provided, single submitter | clinical testing |