Total submissions: 6
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Illumina Laboratory Services, |
RCV000301363 | SCV000373356 | likely benign | Autosomal dominant cerebellar ataxia | 2016-06-14 | criteria provided, single submitter | clinical testing | |
Labcorp Genetics |
RCV000881504 | SCV001024684 | benign | not provided | 2023-12-19 | criteria provided, single submitter | clinical testing | |
Athena Diagnostics | RCV000881504 | SCV001145440 | benign | not provided | 2018-12-27 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002487361 | SCV002797461 | likely benign | Spinocerebellar ataxia type 5; Autosomal recessive spinocerebellar ataxia 14 | 2021-08-06 | criteria provided, single submitter | clinical testing | |
Gene |
RCV000881504 | SCV003840318 | likely benign | not provided | 2021-11-30 | criteria provided, single submitter | clinical testing | See Variant Classification Assertion Criteria. |
Breakthrough Genomics, |
RCV000881504 | SCV005216623 | likely benign | not provided | criteria provided, single submitter | not provided |