List of variants reported as likely benign for blood coagulation disease by ISTH-SSC Genomics in Thrombosis and Hemostasis, KU Leuven, Center for Molecular and Vascular Biology

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000602.5(SERPINE1):c.43G>A (p.Ala15Thr)	rs6092	0.07905
NM_000552.5(VWF):c.6554G>A (p.Arg2185Gln)	rs2229446	0.06069
NM_000552.5(VWF):c.2451T>A (p.His817Gln)	rs57950734	0.03591

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