Total submissions: 6
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000421665 | SCV000519180 | benign | not specified | 2016-02-01 | 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. |
Clinical Genetics DNA and cytogenetics Diagnostics Lab, |
RCV000611171 | SCV000745414 | benign | Hereditary spastic paraplegia 51 | 2017-05-31 | criteria provided, single submitter | clinical testing | |
Labcorp Genetics |
RCV001520601 | SCV001729734 | benign | Spastic paraplegia | 2025-02-03 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV000611171 | SCV001775257 | benign | Hereditary spastic paraplegia 51 | 2021-07-14 | criteria provided, single submitter | clinical testing | |
Breakthrough Genomics, |
RCV004715156 | SCV005295776 | benign | not provided | criteria provided, single submitter | not provided | ||
Diagnostic Laboratory, |
RCV000611171 | SCV000733462 | benign | Hereditary spastic paraplegia 51 | no assertion criteria provided | clinical testing |