C0272315[trait identifier] AND "NIHR Bioresource Rare Diseases, Univer - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 627055	NM_001994.3(F13B):c.299_300insAAC (p.Tyr100Ter)	F13B (Y100*)	Insertion (nonsense)	Coagulation factor deficiency syndrome +1 more	GPathogenic
Select item 68173	NM_000128.4(F11):c.1207G>A (p.Val403Met)	F11 (V403M)	Single nucleotide variant (missense variant)	Hereditary factor XI deficiency disease +1 more	GPathogenic/Likely pathogenic
Select item 627289	NM_000506.5(F2):c.260A>G (p.Tyr87Cys)	F2 (Y87C)	Single nucleotide variant (missense variant)	Coagulation factor deficiency syndrome	GLikely pathogenic

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