List of variants reported as uncertain significance for hemophilia A by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000132.4(F8):c.3169G>A (p.Glu1057Lys)	rs28933673	0.00014
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.1835G>A (p.Arg612His)	rs782473762	0.00001
NM_000132.4(F8):c.6304G>A (p.Gly2102Ser)	rs200433372	0.00001

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