ClinVar Miner

Submissions for variant NM_001303.4(COX10):c.*150_*152del

dbSNP: rs200239586
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000292276 SCV000400633 uncertain significance Mitochondrial complex IV deficiency, nuclear type 1 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000319360 SCV000400634 uncertain significance Leigh syndrome 2016-06-14 criteria provided, single submitter clinical testing

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