Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Ambry Genetics | RCV001266580 | SCV001444756 | likely pathogenic | Inborn genetic diseases | 2019-05-21 | criteria provided, single submitter | clinical testing | |
OMIM | RCV001250911 | SCV001426388 | pathogenic | Arthrogryposis multiplex congenita 5 | 2020-07-31 | no assertion criteria provided | literature only |