ClinVar Miner

Submissions for variant NC_012920.1:m.11899T>C

dbSNP: rs28718242
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics RCV000224384 SCV000280797 likely benign not provided 2015-08-12 criteria provided, single submitter clinical testing Converted during submission to Likely benign.

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