ClinVar Miner

Submissions for variant NM_003482.4(KMT2D):c.11397G>A (p.Gln3799=)

gnomAD frequency: 0.00001  dbSNP: rs751118917
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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 RCV001418448 SCV001620677 likely benign Kabuki syndrome 2023-07-18 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV004531276 SCV004723698 likely benign KMT2D-related disorder 2022-10-03 no assertion criteria provided clinical testing This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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