ClinVar Miner

Submissions for variant NM_001009944.3(PKD1):c.3649G>A (p.Val1217Met)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Clinical Genetics Laboratory, Skane University Hospital Lund RCV004697970 SCV005197160 uncertain significance not provided 2023-07-12 criteria provided, single submitter clinical testing

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