List of variants reported as pathogenic for hemophilia A 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_000132.4(F8):c.6089G>A (p.Ser2030Asn)	rs369414658	0.00009
NM_000132.4(F8):c.2149C>T (p.Arg717Trp)	rs137852435	0.00002
NM_000132.4(F8):c.5302C>T (p.Arg1768Cys)	rs1046670041	0.00001
NM_000132.4(F8):c.2163G>T (p.Met721Ile)	rs1218576358

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