Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Eurofins Ntd Llc |
RCV000724746 | SCV000227985 | uncertain significance | not provided | 2015-04-24 | criteria provided, single submitter | clinical testing | |
Gene |
RCV000724746 | SCV000535595 | likely benign | not provided | 2018-06-01 | criteria provided, single submitter | clinical testing | |
Invitae | RCV002054076 | SCV002381312 | likely benign | Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J | 2023-06-25 | criteria provided, single submitter | clinical testing | |
Ambry Genetics | RCV002426848 | SCV002741994 | likely benign | Cardiovascular phenotype | 2018-09-06 | 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. |