ClinVar Miner

Submissions for variant NM_000504.4(F10):c.829T>A (p.Cys277Ser)

dbSNP: rs2138554252
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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 RCV001420417 SCV001622549 uncertain significance Factor X deficiency 2021-04-28 criteria provided, single submitter research

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