ClinVar Miner

Submissions for variant NM_000130.5(F5):c.3170_3174del (p.Asn1057fs)

dbSNP: rs1571574574
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
NIHR Bioresource Rare Diseases, University of Cambridge RCV000852111 SCV000899669 likely pathogenic Factor V deficiency 2019-02-01 criteria provided, single submitter research

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