"Zotz-Klimas Genetics Lab, MVZ Zotz Klimas"[submitter] AND "F11"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 11891	NM_000128.4(F11):c.403G>T (p.Glu135Ter)	F11 (E135*)	Single nucleotide variant (nonsense)	Hereditary factor XI deficiency disease +2 more	GPathogenic
Select item 2582743	NM_000128.4(F11):c.691A>C (p.Thr231Pro)	F11 (T231P)	Single nucleotide variant (missense variant)	Hereditary factor XI deficiency disease	GUncertain significance
Select item 68197	NM_000128.4(F11):c.723C>G (p.Phe241Leu)	F11 (F241L)	Single nucleotide variant (missense variant)	Hereditary factor XI deficiency disease	GUncertain significance
Select item 550462	NM_000128.4(F11):c.977G>A (p.Arg326His)	F11 (R326H)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely pathogenic
Select item 2582755	NM_000128.4(F11):c.1220C>A (p.Thr407Lys)	F11 (T407K)	Single nucleotide variant (missense variant)	Hereditary factor XI deficiency disease	GUncertain significance
Select item 2582715	NM_000128.4(F11):c.1634G>A (p.Cys545Tyr)	F11, F11-AS1 (C545Y)	Single nucleotide variant (missense variant)	Hereditary factor XI deficiency disease	GUncertain significance

ClinVar