Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV001657893 | SCV001874243 | benign | not provided | 2019-12-29 | criteria provided, single submitter | clinical testing | |
ARUP Laboratories, |
RCV000156988 | SCV000206711 | benign | Noonan syndrome | 2011-09-09 | no assertion criteria provided | clinical testing |