ClinVar Miner

Submissions for variant GRCh37/hg19 6q25.1(chr6:151757398-151757691)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Molecular and Human Genetics, Baylor College of Medicine RCV001195159 SCV001334120 pathogenic Combined oxidative phosphorylation defect type 11 2020-04-16 no assertion criteria provided clinical testing

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