ClinVar Miner

Submissions for variant NM_006766.5(KAT6A):c.5386C>G (p.Pro1796Ala)

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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 RCV004697694 SCV005198507 uncertain significance not provided 2024-02-01 criteria provided, single submitter clinical testing

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