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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 294956	NM_000537.4(REN):c.649G>A (p.Gly217Arg)	REN (G217R)	Single nucleotide variant (missense variant)	not provided +3 more	GBenign/Likely benign
Select item 1712426	NM_000537.4(REN):c.614G>A (p.Arg205Lys)	REN (R205K)	Single nucleotide variant (missense variant)	Kidney disorder	GUncertain significance
Select item 256380	NM_000537.4(REN):c.492+17T>G	REN	Single nucleotide variant (intron variant)	Familial juvenile hyperuricemic nephropathy type 2 +4 more	GBenign
Select item 1712374	NM_000537.4(REN):c.492+6T>C	REN	Single nucleotide variant (intron variant)	Kidney disorder	GUncertain significance
Select item 294959	NM_000537.4(REN):c.492+3A>G	REN	Single nucleotide variant (intron variant)	not provided +4 more	GBenign/Likely benign
Select item 1712359	NM_000537.4(REN):c.443G>A (p.Arg148His)	REN (R148H)	Single nucleotide variant (missense variant)	Kidney disorder +1 more	GUncertain significance
Select item 294964	NM_000537.4(REN):c.22C>G (p.Pro8Ala)	LOC107548112, REN (P8A)	Single nucleotide variant (missense variant)	not provided +4 more	GBenign/Likely benign

ClinVar