List of variants reported as likely pathogenic for Hereditary factor VIII deficiency disease by Mendelics

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000132.4(F8):c.6623A>G (p.Gln2208Arg)	rs782198570	0.00001
NM_000132.4(F8):c.1468A>G (p.Arg490Gly)	rs1603435026
NM_000132.4(F8):c.605G>A (p.Ser202Asn)	rs1603436218
NM_000132.4(F8):c.6301C>G (p.His2101Asp)	rs1603432783

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