ClinVar Miner

Submissions for variant NM_004544.3(NDUFA10):c.-93G>T

gnomAD frequency: 0.00460  dbSNP: rs577432343
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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 RCV000300216 SCV000429026 uncertain significance Leigh syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000350479 SCV000429027 uncertain significance Mitochondrial complex I deficiency 2016-06-14 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV002263607 SCV002544237 likely benign not provided 2024-03-01 criteria provided, single submitter clinical testing NDUFA10: BS2

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