Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
NIHR Bioresource Rare Diseases, |
RCV000504680 | SCV000598723 | likely pathogenic | Leber congenital amaurosis | 2015-01-01 | no assertion criteria provided | research |