Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Baylor Genetics | RCV001329737 | SCV001521257 | uncertain significance | Autosomal recessive nonsyndromic hearing loss 2 | 2020-09-17 | criteria provided, single submitter | clinical testing | This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868]. |
Invitae | RCV002546349 | SCV003448718 | likely benign | not provided | 2024-01-29 | criteria provided, single submitter | clinical testing |