ClinVar Miner

Submissions for variant NC_012920.1:m.9947G>A

dbSNP: rs370688668
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
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 RCV000224665 SCV000281193 benign not provided 2014-10-13 criteria provided, single submitter clinical testing

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