ClinVar Miner

Submissions for variant NM_003482.4(KMT2D):c.13987A>C (p.Arg4663=)

dbSNP: rs2120402557
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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 RCV002182726 SCV002342939 likely benign Kabuki syndrome 2023-04-28 criteria provided, single submitter clinical testing

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