Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Eurofins Ntd Llc |
RCV000731579 | SCV000859417 | uncertain significance | not provided | 2018-01-29 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002493337 | SCV002791434 | uncertain significance | Alagille syndrome due to a NOTCH2 point mutation; Hajdu-Cheney syndrome | 2022-01-03 | criteria provided, single submitter | clinical testing |