Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV000643364 | SCV000765051 | uncertain significance | Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J | 2017-10-04 | criteria provided, single submitter | clinical testing | |
Baylor Genetics | RCV001333486 | SCV001526077 | uncertain significance | Myopathy, myofibrillar, 9, with early respiratory failure | 2018-12-19 | criteria provided, single submitter | clinical testing | This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868]. |