List of variants reported as likely pathogenic for Factor V deficiency by ISTH-SSC Genomics in Thrombosis and Hemostasis, KU Leuven, Center for Molecular and Vascular Biology

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000130.5(F5):c.911G>A (p.Gly304Glu)	rs865947251	0.00002
NM_000130.5(F5):c.5408A>G (p.His1803Arg)	rs754104059	0.00001
NM_000130.5(F5):c.6179G>A (p.Gly2060Asp)	rs1384690038	0.00001
NM_000130.5(F5):c.696C>A (p.Tyr232Ter)

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