ClinVar Miner

Submissions for variant NM_004553.6(NDUFS6):c.67C>T (p.Leu23=)

dbSNP: rs1014264454
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000903277 SCV001047736 benign not provided 2024-01-21 criteria provided, single submitter clinical testing
Natera, Inc. RCV001271672 SCV001452977 likely benign Mitochondrial complex I deficiency 2020-04-20 no assertion criteria provided clinical testing

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