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

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000128.4(F11):c.1288G>A (p.Ala430Thr)	rs753909969	0.00006
NM_000128.4(F11):c.400C>T (p.Gln134Ter)	rs756908183	0.00004
NM_000128.4(F11):c.3G>T (p.Met1Ile)	rs755700350	0.00003
NM_000128.4(F11):c.1432G>A (p.Gly478Arg)	rs542967227	0.00001
NM_000128.4(F11):c.664G>T (p.Asp222Tyr)	rs281875245

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