Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Eurofins Ntd Llc |
RCV000594575 | SCV000709539 | uncertain significance | not provided | 2017-06-22 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002491226 | SCV002806167 | uncertain significance | Alagille syndrome due to a NOTCH2 point mutation; Hajdu-Cheney syndrome | 2021-11-01 | criteria provided, single submitter | clinical testing |