ClinVar Miner

Submissions for variant NM_005006.7(NDUFS1):c.262-15dup

dbSNP: rs34184317
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000360707 SCV000426574 uncertain significance Mitochondrial complex I deficiency 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000268364 SCV000426575 uncertain significance Leigh syndrome 2016-06-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002057638 SCV002371303 benign not provided 2025-01-29 criteria provided, single submitter clinical testing

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