ClinVar Miner

Submissions for variant NM_005006.7(NDUFS1):c.154-10_154-9del

dbSNP: rs568965659
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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 RCV000272442 SCV000426578 uncertain significance Mitochondrial complex I deficiency 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000329832 SCV000426579 uncertain significance Leigh syndrome 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV000676276 SCV001888510 benign not provided 2019-08-09 criteria provided, single submitter clinical testing
Mayo Clinic Laboratories, Mayo Clinic RCV000676276 SCV000802032 benign not provided 2016-02-22 no assertion criteria provided clinical testing

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