ClinVar Miner

Submissions for variant NM_000297.4(PKD2):c.2444A>G (p.Asp815Gly)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Revvity Omics, Revvity RCV003142679 SCV003808412 uncertain significance Polycystic kidney disease 2 2019-05-15 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV003142679 SCV005668067 uncertain significance Polycystic kidney disease 2 2024-05-02 criteria provided, single submitter clinical testing

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