Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Baylor Genetics | RCV001335200 | SCV001528288 | uncertain significance | High myopia-sensorineural deafness syndrome | 2018-07-31 | criteria provided, single submitter | clinical testing | This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868]. |
Fulgent Genetics, |
RCV001335200 | SCV002777582 | uncertain significance | High myopia-sensorineural deafness syndrome | 2021-09-07 | criteria provided, single submitter | clinical testing |