Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
ISCA site 1 | RCV000511368 | SCV000586638 | uncertain significance | See cases | 2016-03-10 | no assertion criteria provided | clinical testing | |
Genome |
RCV000509246 | SCV000607119 | not provided | Becker muscular dystrophy; Duchenne muscular dystrophy | 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. |