Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Counsyl | RCV000671458 | SCV000796434 | uncertain significance | Pendred syndrome | 2017-12-14 | criteria provided, single submitter | clinical testing | |
Invitae | RCV001464496 | SCV001668468 | likely benign | not provided | 2023-11-02 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV001785698 | SCV002027328 | likely benign | Autosomal recessive nonsyndromic hearing loss 4 | 2021-09-05 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV000671458 | SCV002027340 | likely benign | Pendred syndrome | 2021-09-05 | criteria provided, single submitter | clinical testing |