ClinVar Miner

Submissions for variant NM_015512.5(DNAH1):c.6781_6782insG (p.Ser2261fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre RCV004764427 SCV005373825 likely pathogenic Spermatogenic failure 18 2024-09-22 criteria provided, single submitter clinical testing

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