ClinVar Miner

Submissions for variant NM_002495.4(NDUFS4):c.*46G>A (rs567)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000270413 SCV000457896 likely benign Mitochondrial complex I deficiency 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000313869 SCV000457897 likely benign Leigh syndrome 2016-06-14 criteria provided, single submitter clinical testing

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