Total submissions: 6
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Illumina Laboratory Services, |
RCV000293942 | SCV000482986 | benign | Pheochromocytoma | 2016-06-14 | criteria provided, single submitter | clinical testing | |
Gene |
RCV000444699 | SCV000518996 | benign | not specified | 2016-06-01 | 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. |
ARUP Laboratories, |
RCV001810872 | SCV001157663 | benign | not provided | 2019-07-22 | criteria provided, single submitter | clinical testing | |
Center for Genomic Medicine, |
RCV000444699 | SCV002552537 | benign | not specified | 2023-08-15 | criteria provided, single submitter | clinical testing | |
KCCC/NGS Laboratory, |
RCV003316509 | SCV004015424 | benign | Paragangliomas 3 | 2023-07-07 | criteria provided, single submitter | clinical testing | |
Breakthrough Genomics, |
RCV001810872 | SCV005285766 | benign | not provided | criteria provided, single submitter | not provided |