Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Baylor Genetics | RCV001330985 | SCV001522865 | uncertain significance | Autosomal dominant Alport syndrome | 2019-11-21 | criteria provided, single submitter | clinical testing | This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868]. |
Fulgent Genetics, |
RCV002476545 | SCV002793857 | uncertain significance | Autosomal recessive Alport syndrome; Benign familial hematuria | 2022-05-12 | criteria provided, single submitter | clinical testing |