ClinVar Miner

Submissions for variant NM_000132.4(F8):c.670+5G>A

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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 RCV003993644 SCV004809735 uncertain significance Hereditary factor VIII deficiency disease 2024-04-04 criteria provided, single submitter clinical testing

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