Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000833692 | SCV000975456 | benign | not provided | 2018-06-14 | 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. |
Genome- |
RCV001701767 | SCV001933921 | benign | Usher syndrome type 2C | 2021-08-10 | criteria provided, single submitter | clinical testing | |
Genetic Services Laboratory, |
RCV000146083 | SCV000193291 | likely benign | not specified | no assertion criteria provided | clinical testing |