Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Counsyl | RCV000672189 | SCV000797269 | likely pathogenic | Cohen syndrome | 2018-01-18 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV000672189 | SCV005667380 | likely pathogenic | Cohen syndrome | 2024-05-07 | criteria provided, single submitter | clinical testing |