ClinVar Miner

Submissions for variant NM_015488.5(PNKD):c.353-26C>T

gnomAD frequency: 0.00310  dbSNP: rs201632828
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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 RCV000244660 SCV000312555 likely benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001675741 SCV001892294 benign not provided 2021-05-16 criteria provided, single submitter clinical testing

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