List of variants reported as uncertain significance 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: 12

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HGVS	dbSNP	gnomAD frequency
NM_000313.4(PROS1):c.234+72T>C	rs115491294	0.00923
NM_000313.4(PROS1):c.1528G>A (p.Val510Met)	rs138925964	0.00331
NM_000313.4(PROS1):c.227C>T (p.Pro76Leu)	rs73846070	0.00238
NM_000313.4(PROS1):c.1707C>T (p.Ser569=)	rs566166669	0.00005
NM_000313.4(PROS1):c.1594A>G (p.Thr532Ala)	rs371028997	0.00001
NM_000313.4(PROS1):c.988C>T (p.Arg330Trp)	rs536077692	0.00001
NM_000313.4(PROS1):c.1055T>G (p.Ile352Ser)	rs1708455723
NM_000313.4(PROS1):c.1088T>C (p.Leu363Pro)	rs2107150027
NM_000313.4(PROS1):c.1501T>G (p.Ser501Ala)	rs121918472
NM_000313.4(PROS1):c.1544G>A (p.Arg515His)
NM_000313.4(PROS1):c.1916G>T (p.Cys639Phe)
NM_000313.4(PROS1):c.905T>G (p.Leu302Trp)

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