ClinVar Miner

Submissions for variant NM_000505.4(F12):c.169C>G (p.Leu57Val)

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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 RCV003991827 SCV004810126 uncertain significance Factor XII deficiency disease 2024-04-04 criteria provided, single submitter clinical testing

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