List of variants reported as likely pathogenic for blood coagulation disease by Mendelics

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_000133.4(F9):c.1346G>A (p.Arg449Gln)	rs143018900	0.00007
NM_000132.4(F8):c.6623A>G (p.Gln2208Arg)	rs782198570	0.00001
NM_000064.4(C3):c.640C>T (p.Pro214Ser)	rs794729228
NM_000132.4(F8):c.1468A>G (p.Arg490Gly)	rs1603435026
NM_000132.4(F8):c.1752+5G>T	rs2124094299
NM_000132.4(F8):c.605G>A (p.Ser202Asn)	rs1603436218
NM_000132.4(F8):c.6301C>G (p.His2101Asp)	rs1603432783

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