ClinVar Miner

Submissions for variant NC_012920.1:m.10632T>C

dbSNP: rs878888873
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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 RCV000438133 SCV000510800 likely benign not provided 2016-09-14 criteria provided, single submitter clinical testing Converted during submission to Likely benign.

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