Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Eurofins Ntd Llc |
RCV000733482 | SCV000861558 | uncertain significance | not provided | 2018-06-05 | criteria provided, single submitter | clinical testing | |
Invitae | RCV001436792 | SCV001639636 | likely benign | Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J | 2023-07-21 | criteria provided, single submitter | clinical testing | |
Ambry Genetics | RCV002458351 | SCV002616729 | likely benign | Cardiovascular phenotype | 2021-03-18 | criteria provided, single submitter | clinical testing | This alteration is classified as likely benign based on a combination of the following: population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity. |