ClinVar Miner

Submissions for variant NM_000214.3(JAG1):c.387+2T>C

dbSNP: rs1555830919
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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 RCV000514731 SCV000610750 pathogenic not provided 2017-06-28 criteria provided, single submitter clinical testing

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