ClinVar Miner

Submissions for variant NM_001270974.2(HYDIN):c.2702G>T (p.Gly901Val)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Royal Brompton Clinical Genetics And Genomics Laboratory, NHS South East Genomic Laboratory Hub RCV003886347 SCV004704588 uncertain significance Primary ciliary dyskinesia 5 2024-03-06 criteria provided, single submitter clinical testing

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