Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Eurofins Ntd Llc |
RCV000593628 | SCV000700451 | benign | not specified | 2017-02-01 | criteria provided, single submitter | clinical testing | |
Gene |
RCV000833671 | SCV000975435 | likely benign | not provided | 2018-06-12 | 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, |
RCV000833671 | SCV001474388 | benign | not provided | 2019-12-26 | criteria provided, single submitter | clinical testing | |
Center for Genomic Medicine, |
RCV000593628 | SCV002550564 | benign | not specified | 2023-08-15 | criteria provided, single submitter | clinical testing |