Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001327249 | SCV001518315 | likely benign | not provided | 2024-01-08 | criteria provided, single submitter | clinical testing | |
Baylor Genetics | RCV001330106 | SCV001521709 | uncertain significance | Usher syndrome type 2C | 2019-01-21 | criteria provided, single submitter | clinical testing | This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868]. |