List of variants reported as uncertain significance for Protein S deficiency disease by ISTH-SSC Genomics in Thrombosis and Hemostasis, KU Leuven, Center for Molecular and Vascular Biology

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_000313.4(PROS1):c.1095T>G (p.Asn365Lys)	rs199469491	0.00155
NM_000313.4(PROS1):c.284G>A (p.Gly95Glu)	rs144526169	0.00040
NM_000313.4(PROS1):c.*119T>C	rs886058924	0.00026
NM_000313.4(PROS1):c.293C>G (p.Thr98Ser)	rs142805170	0.00011
NM_000313.4(PROS1):c.1088T>C (p.Leu363Pro)	rs2107150027
NM_000313.4(PROS1):c.1568T>C (p.Met523Thr)	rs1483547708

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