Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV000952733 | SCV001099255 | benign | not provided | 2018-05-17 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002502944 | SCV002811766 | likely benign | Prader-Willi syndrome | 2022-05-17 | criteria provided, single submitter | clinical testing | |
Breakthrough Genomics, |
RCV000952733 | SCV005297372 | benign | not provided | criteria provided, single submitter | not provided |