ClinVar Miner

Submissions for variant NM_000132.4(F8):c.6709G>A (p.Ala2237Thr)

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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, King Faisal Specialist Hospital and Research Center RCV004813423 SCV005438318 likely pathogenic Hereditary factor VIII deficiency disease 2024-12-18 criteria provided, single submitter clinical testing

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