ClinVar Miner

Submissions for variant NM_000130.5(F5):c.2232G>C (p.Leu744Phe)

dbSNP: rs2101820303
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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 RCV001420395 SCV001622455 uncertain significance Factor V deficiency 2021-04-28 criteria provided, single submitter research

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