Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Baylor Genetics | RCV001329576 | SCV001521051 | uncertain significance | Autosomal recessive nonsyndromic hearing loss 32 | 2019-04-19 | criteria provided, single submitter | clinical testing | This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868]. |
Invitae | RCV002070160 | SCV002349620 | likely benign | not provided | 2022-03-09 | criteria provided, single submitter | clinical testing |