Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Eurofins Ntd Llc |
RCV000732503 | SCV000860468 | uncertain significance | not provided | 2018-03-27 | criteria provided, single submitter | clinical testing | |
Invitae | RCV001086158 | SCV001017279 | likely benign | Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J | 2022-11-08 | criteria provided, single submitter | clinical testing | |
Ambry Genetics | RCV003344028 | SCV004066442 | likely benign | Cardiovascular phenotype | 2023-07-10 | 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. |