ClinVar Miner

Submissions for variant NM_003482.4(KMT2D):c.11671G>T (p.Ala3891Ser)

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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 RCV003753005 SCV004518488 likely benign Kabuki syndrome 2023-03-27 criteria provided, single submitter clinical testing

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