ClinVar Miner

Submissions for variant NM_000214.3(JAG1):c.1570-28C>G

gnomAD frequency: 0.00425  dbSNP: rs144983462
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000244770 SCV000303009 likely benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001668420 SCV001888490 benign not provided 2015-03-03 criteria provided, single submitter clinical testing

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