List of variants reported as likely pathogenic for hemophilia A by Center For Human Genetics And Laboratory Diagnostics, Dr. Klein, Dr. Rost And Colleagues

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000132.4(F8):c.1835G>A (p.Arg612His)	rs782473762	0.00001
NM_000132.4(F8):c.2045T>C (p.Val682Ala)
NM_000132.4(F8):c.5149T>C (p.Tyr1717His)
NM_000132.4(F8):c.6443A>G (p.Asn2148Ser)	rs1321311878
NM_000132.4(F8):c.6454T>C (p.Ser2152Pro)

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