List of variants reported as likely pathogenic for secondary avascular necrosis by ISTH-SSC Genomics in Thrombosis and Hemostasis, KU Leuven, Center for Molecular and Vascular Biology

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Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_000488.4(SERPINC1):c.1246G>T (p.Ala416Ser)	rs121909548	0.00112
NM_000488.4(SERPINC1):c.218C>T (p.Pro73Leu)	rs121909551	0.00092
NM_000488.4(SERPINC1):c.236G>A (p.Arg79His)	rs121909552	0.00018
NM_000488.4(SERPINC1):c.235C>T (p.Arg79Cys)	rs121909547	0.00005
NM_000488.4(SERPINC1):c.382A>T (p.Asn128Tyr)	rs1657908048	0.00001
NM_000488.4(SERPINC1):c.685C>T (p.Arg229Ter)	rs1657743081	0.00001
NM_000488.4(SERPINC1):c.473T>C (p.Leu158Pro)	rs2102786101
NM_000488.4(SERPINC1):c.550del (p.Thr185fs)	rs1572090173
NM_000488.4(SERPINC1):c.851T>G (p.Met284Arg)	rs1572088737
NM_000488.4(SERPINC1):c.951G>T (p.Leu317Phe)	rs1468108124
NM_000488.4(SERPINC1):c.953C>T (p.Pro318Leu)	rs1460568494

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