ClinVar Miner

Submissions for variant NC_012920.1(MT-CO1):m.6260G>A

dbSNP: rs201395766
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Total submissions: 2
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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 RCV000224938 SCV000281145 likely benign not provided 2015-06-11 criteria provided, single submitter clinical testing Converted during submission to Likely benign.
Athena Diagnostics RCV000224938 SCV001144554 benign not provided 2019-03-22 criteria provided, single submitter clinical testing

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