Total submissions: 7
| Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
|---|---|---|---|---|---|---|---|---|
| Illumina Laboratory Services, |
RCV000020257 | SCV000434232 | benign | Inherited prion disease | 2018-03-06 | criteria provided, single submitter | clinical testing | This variant was observed in the ICSL laboratory as part of a predisposition screen in an ostensibly healthy population. It had not been previously curated by ICSL or reported in the Human Gene Mutation Database (HGMD: prior to June 1st, 2018), and was therefore a candidate for classification through an automated scoring system. Utilizing variant allele frequency, disease prevalence and penetrance estimates, and inheritance mode, an automated score was calculated to assess if this variant is too frequent to cause the disease. Based on the score and internal cut-off values, a variant classified as benign is not then subjected to further curation. The score for this variant resulted in a classification of benign for this disease. |
| Labcorp Genetics |
RCV000873683 | SCV001015725 | benign | Huntington disease-like 1 | 2024-01-19 | criteria provided, single submitter | clinical testing | |
| ARUP Laboratories, |
RCV001573203 | SCV001474173 | benign | not provided | 2022-02-05 | criteria provided, single submitter | clinical testing | |
| Breakthrough Genomics, |
RCV001573203 | SCV005309448 | benign | not provided | criteria provided, single submitter | not provided | ||
| OMIM | RCV004577713 | SCV000034599 | uncertain significance | Reclassified - variant of unknown significance | 2012-02-01 | no assertion criteria provided | literature only | |
| Laboratory of Diagnostic Genome Analysis, |
RCV001573203 | SCV001798698 | likely benign | not provided | no assertion criteria provided | clinical testing | ||
| Genome Diagnostics Laboratory, |
RCV001573203 | SCV001807093 | likely benign | not provided | no assertion criteria provided | clinical testing |