ClinVar Miner

Submissions for variant NM_001303052.2(MYT1L):c.1751del (p.Lys584fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Genetics laboratory, Necker Hospital RCV003325403 SCV004031403 pathogenic not provided 2021-07-26 no assertion criteria provided clinical testing

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