List of variants reported as pathogenic for Factor X deficiency

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Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_000504.4(F10):c.424G>A (p.Glu142Lys)	rs61753266	0.00347
NM_000504.4(F10):c.1012G>A (p.Val338Met)	rs121964947	0.00001
NM_000504.4(F10):c.1073C>T (p.Thr358Met)	rs768222784	0.00001
NM_000504.4(F10):c.140A>G (p.Glu47Gly)	rs121964943	0.00001
NM_000504.4(F10):c.161A>G (p.Glu54Gly)	rs121964944	0.00001
NM_000504.4(F10):c.1096C>T (p.Arg366Cys)	rs104894392
NM_000504.4(F10):c.1120T>C (p.Ser374Pro)	rs121964941
NM_000504.4(F10):c.160G>A (p.Glu54Lys)	rs121964939
NM_000504.4(F10):c.214G>C (p.Glu72Gln)	rs121964945
NM_000504.4(F10):c.307G>C (p.Asp103His)
NM_000504.4(F10):c.513del (p.Cys172fs)	rs2138548669
NM_000504.4(F10):c.61G>A (p.Gly21Arg)	rs753790195
NM_000504.4(F10):c.814del (p.Ile271_Leu272insTer)	rs387906506
NM_000504.4(F10):c.859A>T (p.Arg287Trp)	rs121964948
NM_000504.4(F10):c.964G>A (p.Asp322Asn)	rs121964942
NM_001312675.2(F10):c.*138C>T	rs121964940

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