ClinVar Miner

Submissions for variant NM_019616.4(F7):c.783_799del (p.Arg262fs)

dbSNP: rs786205091
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000012858 SCV000033099 pathogenic Factor VII deficiency 1994-07-01 no assertion criteria provided literature only
ISTH-SSC Genomics in Thrombosis and Hemostasis, KU Leuven, Center for Molecular and Vascular Biology RCV002243639 SCV002515621 pathogenic Congenital factor VII deficiency no assertion criteria provided research

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