ClinVar Miner

Submissions for variant NM_004933.3(CDH15):c.955G>A (p.Glu319Lys)

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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 RCV004813360 SCV005438206 uncertain significance von Willebrand disease type 1 2024-12-17 criteria provided, single submitter clinical testing

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