Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Counsyl | RCV000673329 | SCV000798517 | uncertain significance | Autosomal recessive nonsyndromic hearing loss 2; Usher syndrome type 1 | 2018-03-19 | criteria provided, single submitter | clinical testing | |
Baylor Genetics | RCV001334333 | SCV001527146 | uncertain significance | Autosomal dominant nonsyndromic hearing loss 11 | 2018-12-21 | criteria provided, single submitter | clinical testing | This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868]. |