ClinVar Miner

Submissions for variant NM_014727.3(KMT2B):c.1918T>A (p.Ser640Thr)

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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 RCV002575808 SCV002931750 likely benign not provided 2024-04-13 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV002575808 SCV004145452 uncertain significance not provided 2022-12-01 criteria provided, single submitter clinical testing

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