Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Baylor Genetics | RCV001336876 | SCV001530388 | uncertain significance | Autosomal dominant nonsyndromic hearing loss 13 | 2018-01-24 | criteria provided, single submitter | clinical testing | This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868]. |
Invitae | RCV003770867 | SCV004611531 | likely benign | not provided | 2023-12-25 | criteria provided, single submitter | clinical testing |