ClinVar Miner

Submissions for variant NM_001377299.1(NDUFS2):c.*78GT[16]

dbSNP: rs10629771
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000260184 SCV000350141 uncertain significance Mitochondrial complex I deficiency 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001712008 SCV001944407 benign not provided 2019-08-13 criteria provided, single submitter clinical testing

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