ClinVar Miner

Submissions for variant NM_001303.4(COX10):c.929-9_929-7dup

dbSNP: rs144296730
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000399268 SCV000400621 likely benign Leigh syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000297390 SCV000400622 likely benign Mitochondrial complex IV deficiency, nuclear type 1 2016-06-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001518767 SCV001727524 benign not provided 2024-02-01 criteria provided, single submitter clinical testing
GeneDx RCV001518767 SCV001857218 benign not provided 2015-03-03 criteria provided, single submitter clinical testing

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