ClinVar Miner

Submissions for variant NM_003482.4(KMT2D):c.9932A>G (p.Gln3311Arg)

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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 RCV005080839 SCV005716186 benign Kabuki syndrome 2024-03-14 criteria provided, single submitter clinical testing

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