ClinVar Miner

Submissions for variant NM_001109809.5(ZFP57):c.352+15G>T

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV003120123 SCV003799636 likely benign Diabetes mellitus, transient neonatal, 1 2022-03-23 criteria provided, single submitter clinical testing

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