List of variants reported as likely pathogenic for Thrombophilia due to protein S deficiency, autosomal dominant 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.200A>C (p.Glu67Ala)	rs766423432	0.00002
NM_000313.4(PROS1):c.1337T>C (p.Leu446Pro)	rs2107137626
NM_000313.4(PROS1):c.1501T>C (p.Ser501Pro)	rs121918472
NM_000313.4(PROS1):c.1862G>T (p.Gly621Val)	rs2107124949
NM_000313.4(PROS1):c.346+1G>T
NM_000313.4(PROS1):c.49dup (p.Leu17fs)	rs1575904540

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