List of variants studied for hemophilia A by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

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		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_000132.4(F8):c.396A>C (p.Glu132Asp)	rs137852388	0.00018
NM_000132.4(F8):c.3169G>A (p.Glu1057Lys)	rs28933673	0.00014
NM_000132.4(F8):c.6089G>A (p.Ser2030Asn)	rs369414658	0.00009
NM_000132.4(F8):c.2840C>G (p.Pro947Arg)	rs782318401	0.00005
NM_000132.4(F8):c.4828G>T (p.Ala1610Ser)	rs782127226	0.00004
NM_000132.4(F8):c.2149C>T (p.Arg717Trp)	rs137852435	0.00002
NM_000132.4(F8):c.1835G>A (p.Arg612His)	rs782473762	0.00001
NM_000132.4(F8):c.5302C>T (p.Arg1768Cys)	rs1046670041	0.00001
NM_000132.4(F8):c.6304G>A (p.Gly2102Ser)	rs200433372	0.00001
NM_000132.4(F8):c.2163G>T (p.Met721Ile)	rs1218576358

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