List of variants reported as pathogenic for Hereditary factor XI deficiency disease by NIHR Bioresource Rare Diseases, University of Cambridge

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Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_000128.4(F11):c.403G>T (p.Glu135Ter)	rs121965063	0.00066
NM_000128.4(F11):c.901T>C (p.Phe301Leu)	rs121965064	0.00065
NM_000128.4(F11):c.1288G>A (p.Ala430Thr)	rs753909969	0.00006
NM_000128.4(F11):c.802C>T (p.Arg268Cys)	rs763496524	0.00005
NM_000128.4(F11):c.1432G>A (p.Gly478Arg)	rs542967227	0.00001
NM_000128.4(F11):c.365G>A (p.Gly122Asp)	rs369650561	0.00001
NM_000128.4(F11):c.755+2T>C	rs1220869989	0.00001
NM_000128.4(F11):c.1325del (p.Leu442fs)	rs757530565
NM_000128.4(F11):c.1782C>A (p.Ser594Arg)	rs28934609

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