C1842982[trait identifier] AND "Revvity Omics, Revvity"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2439815	NM_012120.3(CD2AP):c.721C>A (p.Pro241Thr)	CD2AP (P241T)	Single nucleotide variant (missense variant)	Focal segmental glomerulosclerosis 3, susceptibility to	GUncertain significance
Select item 402519	NM_012120.3(CD2AP):c.902A>T (p.Lys301Met)	CD2AP (K301M)	Single nucleotide variant (missense variant)	Focal segmental glomerulosclerosis 3, susceptibility to +2 more	GUncertain significance