ClinVar Miner

Submissions for variant NM_000128.4(F11):c.230T>C (p.Val77Ala)

dbSNP: rs1433941674
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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 RCV001420443 SCV001622479 uncertain significance Hereditary factor XI deficiency disease 2021-04-28 criteria provided, single submitter research

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