ClinVar Miner

Submissions for variant NM_003482.4(KMT2D):c.1153C>T (p.Pro385Ser)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003069724 SCV003471703 benign Kabuki syndrome 2023-12-11 criteria provided, single submitter clinical testing

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