Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Centre for Mendelian Genomics, |
RCV000415277 | SCV000492711 | likely pathogenic | Ocular albinism | 2015-10-30 | criteria provided, single submitter | clinical testing |