ClinVar Miner

Submissions for variant NM_002528.7(NTHL1):c.792-39C>T

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV003494155 SCV004242661 likely benign not specified 2025-03-04 criteria provided, single submitter clinical testing

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