List of variants reported as pathogenic for Hereditary factor XI deficiency disease by Fulgent Genetics, Fulgent Genetics

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Total variants: 11

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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.438C>A (p.Cys146Ter)	rs121965066	0.00005
NM_000128.4(F11):c.1107C>A (p.Tyr369Ter)	rs773905328	0.00003
NM_000128.4(F11):c.1489C>T (p.Arg497Ter)	rs375422404	0.00003
NM_000128.4(F11):c.1556G>A (p.Trp519Ter)	rs201007090	0.00001
NM_000128.4(F11):c.67C>T (p.Gln23Ter)	rs768409400	0.00001
NM_000128.4(F11):c.841C>T (p.Gln281Ter)	rs770505620	0.00001
NM_000128.4(F11):c.1075del (p.Ile359fs)	rs786204429
NM_000128.4(F11):c.1234C>T (p.Gln412Ter)	rs538083600
NM_000128.4(F11):c.1313C>A (p.Ser438Ter)	rs786204724

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