Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Eurofins Ntd Llc |
RCV000595906 | SCV000708452 | uncertain significance | not provided | 2017-05-09 | criteria provided, single submitter | clinical testing | |
Ambry Genetics | RCV000620212 | SCV000735899 | likely benign | Cardiovascular phenotype | 2017-06-05 | 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. |
Invitae | RCV001495203 | SCV001699873 | likely benign | Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J | 2023-02-21 | criteria provided, single submitter | clinical testing | |
Gene |
RCV000595906 | SCV001861443 | likely benign | not provided | 2021-03-03 | criteria provided, single submitter | clinical testing |