ClinVar Miner

Submissions for variant NM_001009944.3(PKD1):c.1325C>T (p.Ala442Val)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Blueprint Genetics RCV000788478 SCV000927610 uncertain significance not provided 2018-03-27 criteria provided, single submitter clinical testing

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