List of variants reported as likely pathogenic for inherited thrombophilia by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000312.4(PROC):c.565C>T (p.Arg189Trp)	rs146922325	0.00046
NM_000313.4(PROS1):c.233C>T (p.Thr78Met)	rs6122	0.00002
NM_000312.4(PROC):c.1321T>C (p.Tyr441His)	rs753436021	0.00001
NM_000312.4(PROC):c.982C>T (p.Arg328Cys)	rs201907715

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