Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
NIHR Bioresource Rare Diseases, |
RCV000851790 | SCV000899741 | uncertain significance | Hereditary von Willebrand disease | 2019-02-01 | criteria provided, single submitter | research | |
Quest Diagnostics Nichols Institute San Juan Capistrano | RCV001284373 | SCV001470128 | uncertain significance | not provided | 2020-03-20 | criteria provided, single submitter | clinical testing |