ClinVar Miner

Submissions for variant NM_000130.5(F5):c.3577del (p.Gln1192_Val1193insTer)

dbSNP: rs2101818861
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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 RCV001420391 SCV001622451 likely pathogenic Factor V deficiency 2021-04-28 criteria provided, single submitter research

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