ClinVar Miner

List of variants reported as likely pathogenic for Congenital factor VII deficiency by Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_019616.4(F7):c.854G>A (p.Arg285His)	rs121964929	0.00009
NM_019616.4(F7):c.1085C>T (p.Thr362Met)	rs531225271	0.00008
NM_019616.4(F7):c.196C>T (p.Arg66Trp)

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