"FPR1-related condition"[Disease/phenotype] AND "PreventionGenetics, p - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3040106	NM_002029.4(FPR1):c.1038G>A (p.Glu346=)	FPR1	Single nucleotide variant (synonymous variant)	FPR1-related condition	GLikely benign
Select item 1147556	NM_002029.4(FPR1):c.858A>G (p.Thr286=)	FPR1	Single nucleotide variant (synonymous variant)	FPR1-related condition +1 more	GLikely benign
Select item 712949	NM_002029.4(FPR1):c.822C>T (p.Gly274=)	FPR1	Single nucleotide variant (synonymous variant)	FPR1-related condition +1 more	GBenign/Likely benign
Select item 526511	NM_002029.4(FPR1):c.806G>A (p.Arg269His)	FPR1 (R269H)	Single nucleotide variant (missense variant)	Gingival disorder +1 more	GBenign
Select item 2066974	NM_002029.4(FPR1):c.726C>A (p.Val242=)	FPR1	Single nucleotide variant (synonymous variant)	FPR1-related condition +1 more	GLikely benign
Select item 526512	NM_002029.4(FPR1):c.645C>T (p.Ser215=)	FPR1	Single nucleotide variant (synonymous variant)	Gingival disorder +1 more	GBenign
Select item 456367	NM_002029.4(FPR1):c.488G>A (p.Arg163His)	FPR1 (R163H)	Single nucleotide variant (missense variant)	FPR1-related condition +1 more	GBenign/Likely benign
Select item 785829	NM_002029.4(FPR1):c.368G>A (p.Arg123His)	FPR1 (R123H)	Single nucleotide variant (missense variant)	FPR1-related condition +1 more	GLikely benign
Select item 526514	NM_002029.4(FPR1):c.289C>A (p.Leu97Met)	FPR1 (L97M)	Single nucleotide variant (missense variant)	Gingival disorder +1 more	GBenign

ClinVar