ClinVar Miner

Submissions for variant NC_012920.1(MT-CYB):m.16182_16183del

dbSNP: rs371240719
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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 Pediatrics, Division of Medical Genetics, Faculty of Medicine Ramathibodi Hospital, Mahidol University RCV002051604 SCV002107183 uncertain significance Mitochondrial inheritance no assertion criteria provided research

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