List of variants reported as uncertain significance for congenital factor X deficiency by Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center

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Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_000504.4(F10):c.80G>A (p.Arg27His)	rs1263735827	0.00001
NM_000504.4(F10):c.107C>A (p.Ala36Glu)	rs2036405879
NM_000504.4(F10):c.1325G>A (p.Gly442Asp)	rs1233330150
NM_000504.4(F10):c.1387G>C (p.Asp463His)	rs1476602298
NM_000504.4(F10):c.152G>A (p.Gly51Glu)	rs751782758
NM_000504.4(F10):c.28C>T (p.Leu10Phe)	rs2142244681
NM_000504.4(F10):c.829T>A (p.Cys277Ser)	rs2138554252
NM_000504.4(F10):c.84G>T (p.Arg28Ser)	rs1212018525
NM_000504.4(F10):c.89A>G (p.Gln30Arg)	rs2142252077

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