Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Ce |
RCV000513473 | SCV000608462 | uncertain significance | not provided | 2017-04-01 | criteria provided, single submitter | clinical testing | |
Genome |
RCV000509196 | SCV000607065 | not provided | Kufor-Rakeb syndrome | no assertion provided | phenotyping only | GenomeConnect assertions are reported exactly as they appear on the patient-provided report from the testing laboratory. GenomeConnect staff make no attempt to reinterpret the clinical significance of the variant. |