ClinVar Miner

Submissions for variant NM_003482.4(KMT2D):c.9807G>T (p.Gln3269His)

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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 RCV003753626 SCV004533152 benign Kabuki syndrome 2023-08-19 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV005013155 SCV005636432 uncertain significance Kabuki syndrome 1; Choanal atresia-athelia-hypothyroidism-delayed puberty-short stature syndrome 2024-03-07 criteria provided, single submitter clinical testing

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