"Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, E - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1299830	NM_003661.4(APOL1):c.318T>C (p.Asn106=)	APOL1	Single nucleotide variant (synonymous variant)	Focal segmental glomerulosclerosis 4, susceptibility to +2 more	GLikely benign
Select item 729570	NM_003661.4(APOL1):c.472C>T (p.Leu158Phe)	APOL1 (L158F +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 717758	NM_003661.4(APOL1):c.573C>T (p.Leu191=)	APOL1	Single nucleotide variant (synonymous variant)	Focal segmental glomerulosclerosis 4, susceptibility to +1 more	GBenign/Likely benign
Select item 1170737	NM_003661.4(APOL1):c.792C>A (p.Asn264Lys)	APOL1 (N246K +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 731686	NM_003661.4(APOL1):c.809G>A (p.Gly270Asp)	APOL1 (G270D +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 1284893	NM_003661.4(APOL1):c.851G>A (p.Arg284His)	APOL1 (R266H +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign/Likely benign
Select item 727880	NM_003661.4(APOL1):c.945T>G (p.Gly315=)	APOL1	Single nucleotide variant (synonymous variant)	Focal segmental glomerulosclerosis 4, susceptibility to +1 more	GLikely benign

ClinVar