List of variants reported as pathogenic for congenital factor VII deficiency by Fulgent Genetics, Fulgent Genetics

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_019616.4(F7):c.1025G>A (p.Arg342Gln)	rs121964926	0.00118
NM_019616.4(F7):c.364+1G>A	rs1056071555	0.00006
NM_019616.4(F7):c.845C>T (p.Ala282Val)	rs121964931	0.00006
NM_019616.4(F7):c.1043G>T (p.Cys348Phe)	rs121964927	0.00001
NM_019616.4(F7):c.1008G>A (p.Met336Ile)
NM_019616.4(F7):c.1157A>G (p.His386Arg)
NM_019616.4(F7):c.225+1G>C	rs1566906827

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