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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 718615	NM_020381.4(PDSS2):c.1146G>A (p.Ser382=)	PDSS2	Single nucleotide variant (synonymous variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1496856	NM_020381.4(PDSS2):c.908A>G (p.Glu303Gly)	PDSS2 (E303G)	Single nucleotide variant (missense variant)	Kidney disorder +2 more	GUncertain significance
Select item 214987	NM_020381.4(PDSS2):c.667G>A (p.Val223Ile)	PDSS2 (V223I)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 1712477	NM_020381.4(PDSS2):c.290C>T (p.Thr97Ile)	PDSS2 (T97I)	Single nucleotide variant (missense variant)	Kidney disorder	GUncertain significance
Select item 1712403	NM_020381.4(PDSS2):c.31C>T (p.Pro11Ser)	PDSS2 (P11S)	Single nucleotide variant (missense variant)	Focal segmental glomerulosclerosis	GUncertain significance
Select item 138690	NM_020381.4(PDSS2):c.11G>C (p.Arg4Pro)	PDSS2 (R4P)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign
Select item 138689	NM_020381.4(PDSS2):c.7T>C (p.Phe3Leu)	PDSS2 (F3L)	Single nucleotide variant (missense variant)	Kidney disorder +2 more	GBenign

ClinVar