List of variants reported as uncertain significance 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_000130.5(F5):c.5054C>G (p.Thr1685Ser)	rs6011	0.00144
NM_000130.5(F5):c.5245C>G (p.Leu1749Val)	rs6034	0.00144
NM_000130.5(F5):c.2321G>C (p.Gly774Ala)	rs547915978	0.00001
NM_000130.5(F5):c.6644G>A (p.Arg2215His)	rs952196842	0.00001
NM_000130.5(F5):c.1321C>G (p.Arg441Gly)	rs747006175
NM_000130.5(F5):c.6122T>G (p.Ile2041Ser)	rs1364834534
NM_000130.5(F5):c.986G>A (p.Cys329Tyr)	rs574459300

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