Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Illumina Clinical Services Laboratory, |
RCV000355295 | SCV000350266 | likely benign | Pheochromocytoma | 2016-06-14 | criteria provided, single submitter | clinical testing | |
Gene |
RCV000828442 | SCV000970130 | likely benign | not provided | 2018-05-31 | 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. |