Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Eurofins Ntd Llc |
RCV000734016 | SCV000862126 | uncertain significance | not provided | 2018-07-11 | criteria provided, single submitter | clinical testing | |
Baylor Genetics | RCV001331991 | SCV001524170 | uncertain significance | Autosomal recessive nonsyndromic hearing loss 9 | 2019-03-11 | criteria provided, single submitter | clinical testing | This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868]. |