C4746745[trait identifier] AND "Genetic Diagnostic Laboratory, Univers - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 424759	NM_000092.4(COL4A4):c.[1320_1369+2del];[2320G>C]			Autosomal recessive Alport syndrome	GPathogenic
Select item 424758	NM_000091.4(COL4A3):c.[3490G>T];[687G>A]			Autosomal recessive Alport syndrome	GPathogenic