"F2-related condition"[Disease/phenotype] AND "PreventionGenetics, par - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2631315	NM_000506.5(F2):c.454_457del (p.Leu152fs)	F2 (L152fs)	Deletion (frameshift variant)	F2-related condition	GLikely pathogenic
Select item 2884634	NM_000506.5(F2):c.648T>G (p.Asp216Glu)	F2 (D216E)	Single nucleotide variant (missense variant)	F2-related condition +1 more	GLikely benign
Select item 304811	NM_000506.5(F2):c.813C>T (p.Gly271=)	F2	Single nucleotide variant (synonymous variant)	Thrombophilia due to thrombin defect +2 more	GConflicting classifications of pathogenicity
Select item 2632426	NM_000506.5(F2):c.1084G>A (p.Gly362Arg)	F2 (G362R)	Single nucleotide variant (missense variant)	F2-related condition	GUncertain significance
Select item 2630243	NM_000506.5(F2):c.1472+3G>C	F2	Single nucleotide variant (intron variant)	F2-related condition	GUncertain significance
Select item 1775708	NM_000506.5(F2):c.1581C>T (p.Asn527=)	F2	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +2 more	GLikely benign
Select item 2629094	NM_000506.5(F2):c.1598G>C (p.Arg533Pro)	F2 (R533P)	Single nucleotide variant (missense variant)	F2-related condition	GUncertain significance

ClinVar