ClinVar Miner

List of variants reported as likely pathogenic for Congenital factor VII deficiency by Genetics and Molecular Pathology, SA Pathology

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_019616.4(F7):c.995C>T (p.Ala332Val)	rs36209567	0.00038
NM_019616.4(F7):c.1043G>T (p.Cys348Phe)	rs121964927	0.00001
NM_019616.4(F7):c.748G>A (p.Asp250Asn)

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