Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Baylor Genetics | RCV001329738 | SCV001521258 | uncertain significance | Autosomal recessive nonsyndromic hearing loss 2 | 2019-12-10 | criteria provided, single submitter | clinical testing | This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868]. |
Revvity Omics, |
RCV003132422 | SCV003817841 | uncertain significance | not provided | 2023-08-08 | criteria provided, single submitter | clinical testing |