"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "CFB"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2179396	NM_001710.6(CFB):c.236C>T (p.Thr79Met)	CFB (T79M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1693908	NM_001710.6(CFB):c.322G>A (p.Asp108Asn)	CFB (D108N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 356279	NM_001710.6(CFB):c.724A>C (p.Ile242Leu)	CFB (I242L)	Single nucleotide variant (missense variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 2682921	NM_001710.6(CFB):c.1142G>A (p.Arg381His)	CFB (R381H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1513767	NM_001710.6(CFB):c.1862A>G (p.Glu621Gly)	CFB (E621G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1693909	NM_001710.6(CFB):c.2199G>C (p.Gln733His)	CFB (Q733H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1369628	NM_001710.6(CFB):c.2272G>A (p.Asp758Asn)	CFB (D758N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

ClinVar