Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV001610466 | SCV001832852 | benign | not provided | 2018-06-23 | criteria provided, single submitter | clinical testing | |
ARUP Laboratories, |
RCV000156994 | SCV000206718 | benign | Noonan syndrome | 2010-12-23 | no assertion criteria provided | clinical testing |