Total submissions: 5
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Eurofins Ntd Llc |
RCV000366351 | SCV000341812 | uncertain significance | not provided | 2016-06-07 | criteria provided, single submitter | clinical testing | |
Invitae | RCV000366351 | SCV000640358 | benign | not provided | 2024-01-14 | criteria provided, single submitter | clinical testing | |
Gene |
RCV000366351 | SCV000978085 | benign | not provided | 2018-04-30 | 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. |
Laboratory of Diagnostic Genome Analysis, |
RCV000366351 | SCV002036558 | likely benign | not provided | no assertion criteria provided | clinical testing | ||
Clinical Genetics DNA and cytogenetics Diagnostics Lab, |
RCV000366351 | SCV002038152 | likely benign | not provided | no assertion criteria provided | clinical testing |