Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV001722614 | SCV000716363 | likely benign | not provided | 2018-04-30 | criteria provided, single submitter | clinical testing | |
Genome |
RCV000845019 | SCV000986852 | not provided | Neurodevelopmental and congenital anomalies | no assertion provided | phenotyping only | Variant interpretted as Uncertain significance and reported on 04/10/2018 by GTR ID Illumina Clinical Services Laboratory. 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. |