"APOL1-associated kidney disease"[Disease/phenotype] AND "Clinical Gen - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 277678	NM_003661.4(APOL1):c.1024A>G (p.Ser342Gly)	APOL1 (S358G +2 more)	Single nucleotide variant (missense variant)	APOL1-associated kidney disease +3 more	GConflicting classifications of pathogenicity; risk factor
Select item 127198	NM_003661.4(APOL1):c.1152T>G (p.Ile384Met)	APOL1 (I400M +2 more)	Single nucleotide variant (missense variant)	APOL1-associated kidney disease +3 more	GConflicting classifications of pathogenicity; risk factor