Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000540278 | SCV000642701 | uncertain significance | Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J | 2017-08-26 | criteria provided, single submitter | clinical testing | |
Eurofins Ntd Llc |
RCV000592077 | SCV000702985 | uncertain significance | not provided | 2016-11-29 | criteria provided, single submitter | clinical testing | |
Gene |
RCV000592077 | SCV000975029 | likely benign | not provided | 2018-06-20 | criteria provided, single submitter | clinical testing | This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease. |
Women's Health and Genetics/Laboratory Corporation of America, |
RCV003330772 | SCV004038602 | uncertain significance | not specified | 2023-08-19 | criteria provided, single submitter | clinical testing |