"Center for Genomic Medicine, King Faisal Specialist Hospital and Rese - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1098464	NM_001994.3(F13B):c.1693G>A (p.Ala565Thr)	F13B (A565T)	Single nucleotide variant (missense variant)	Factor XIII, b subunit, deficiency of	GUncertain significance
Select item 1098465	NM_001994.3(F13B):c.881A>T (p.His294Leu)	F13B (H294L)	Single nucleotide variant (missense variant)	Factor XIII, b subunit, deficiency of	GUncertain significance
Select item 1098466	NM_001994.3(F13B):c.779G>T (p.Trp260Leu)	F13B (W260L)	Single nucleotide variant (missense variant)	Factor XIII, b subunit, deficiency of	GUncertain significance
Select item 1098467	NM_001994.3(F13B):c.625A>G (p.Thr209Ala)	F13B (T209A)	Single nucleotide variant (missense variant)	Factor XIII, b subunit, deficiency of	GUncertain significance
Select item 1098468	NM_001994.3(F13B):c.565G>T (p.Gly189Ter)	F13B (G189*)	Single nucleotide variant (nonsense)	Factor XIII, b subunit, deficiency of	GPathogenic
Select item 1098469	NM_001994.3(F13B):c.521A>T (p.Asp174Val)	F13B (D174V)	Single nucleotide variant (missense variant)	Factor XIII, b subunit, deficiency of	GUncertain significance
Select item 1098470	NM_001994.3(F13B):c.431C>T (p.Pro144Leu)	F13B (P144L)	Single nucleotide variant (missense variant)	Factor XIII, b subunit, deficiency of	GUncertain significance

ClinVar