Total submissions: 7
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000117171 | SCV000519414 | benign | not specified | 2016-01-07 | 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. |
Athena Diagnostics | RCV000711872 | SCV000842279 | benign | not provided | 2017-04-20 | criteria provided, single submitter | clinical testing | |
Ambry Genetics | RCV002312121 | SCV000846081 | benign | Inborn genetic diseases | 2015-12-31 | criteria provided, single submitter | clinical testing | This alteration is classified as benign based on a combination of the following: seen in unaffected individuals, 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 | RCV001519887 | SCV001728847 | benign | Intellectual disability, autosomal dominant 8 | 2024-02-01 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV001519887 | SCV001933964 | benign | Intellectual disability, autosomal dominant 8 | 2021-08-10 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV001701670 | SCV001933965 | benign | Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal recessive | 2021-08-10 | criteria provided, single submitter | clinical testing | |
Genetic Services Laboratory, |
RCV000117171 | SCV000151335 | likely benign | not specified | no assertion criteria provided | clinical testing | Likely benign based on allele frequency in 1000 Genomes Project or ESP global frequency and its presence in a patient with a rare or unrelated disease phenotype. NOT Sanger confirmed. |