ClinVar Miner

Submissions for variant NM_170606.3(KMT2C):c.8957G>A (p.Gly2986Asp)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Revvity Omics, Revvity RCV003133916 SCV003810112 uncertain significance Kleefstra syndrome 2 2020-11-05 criteria provided, single submitter clinical testing

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