ClinVar Miner

Submissions for variant NM_003482.4(KMT2D):c.10944G>A (p.Pro3648=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003072619 SCV003471414 likely benign Kabuki syndrome 2023-08-04 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003389916 SCV004130729 likely benign not provided 2022-06-01 criteria provided, single submitter clinical testing KMT2D: BP4, BP7

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