ClinVar Miner

Submissions for variant NM_004544.4(NDUFA10):c.*1894_*1914delinsGGG

dbSNP: rs886055819
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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 RCV000330773 SCV000428952 uncertain significance Leigh syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000383047 SCV000428953 uncertain significance Mitochondrial complex I deficiency 2016-06-14 criteria provided, single submitter clinical testing

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