"Genome Diagnostics Laboratory, The Hospital for Sick Children"[submit - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 774281	NM_021023.6(CFHR3):c.53G>C (p.Gly18Ala)	CFHR3 (G18A)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 730391	NM_021023.6(CFHR3):c.101T>G (p.Phe34Cys)	CFHR3 (F34C)	Single nucleotide variant (missense variant)	Age related macular degeneration 1 +3 more	GBenign/Likely benign
Select item 1712376	NM_021023.6(CFHR3):c.355G>C (p.Gly119Arg)	CFHR3 (G119R)	Single nucleotide variant (missense variant)	Kidney disorder	GUncertain significance

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