List of variants reported as benign for Hereditary factor XI deficiency disease

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Total variants: 19

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HGVS	dbSNP	gnomAD frequency
NM_000128.4(F11):c.*479A>T	rs1062547	0.40400
NM_000128.4(F11):c.*296G>C	rs4253430	0.39990
NM_000128.3(F11):c.-316C>G	rs3733403	0.18163
NM_000128.4(F11):c.*265A>G	rs4253429	0.16938
NM_000128.4(F11):c.*852G>A	rs4253431	0.16273
NM_000128.4(F11):c.1191T>C (p.Gly397=)	rs5970	0.16228
NM_000128.4(F11):c.801A>G (p.Thr267=)	rs5974	0.16187
NM_000128.4(F11):c.*322G>A	rs4253865	0.07317
NM_000128.4(F11):c.1812G>T (p.Arg604=)	rs5971	0.06917
NM_000128.4(F11):c.429C>T (p.Asp143=)	rs5973	0.06445
NM_000128.4(F11):c.1839G>A (p.Glu613=)	rs5976	0.04596
NM_000128.4(F11):c.1707C>T (p.Asp569=)	rs5975	0.02893
NM_000128.4(F11):c.*885G>A	rs4253432	0.01236
NM_000128.4(F11):c.731A>G (p.Gln244Arg)	rs5969	0.00564
NM_000128.4(F11):c.*1A>G	rs143899287	0.00378
NM_000128.4(F11):c.*175C>T	rs148610742	0.00153
NM_000128.4(F11):c.539A>G (p.Lys180Arg)	rs190283743	0.00036
NM_000128.4(F11):c.*186C>T	rs142128633	0.00004
NM_000128.4(F11):c.-1-138A>C	rs3822057

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