ClinVar Miner

Submissions for variant NM_004544.3(NDUFA10):c.-87A>C

gnomAD frequency: 0.00031  dbSNP: rs886055827
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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 RCV000379454 SCV000429022 uncertain significance Mitochondrial complex I deficiency 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000279233 SCV000429023 uncertain significance Leigh syndrome 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004694541 SCV005187460 uncertain significance not provided criteria provided, single submitter not provided

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