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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1712474	NM_004998.4(MYO1E):c.*716A>G	MYO1E	Single nucleotide variant (3 prime UTR variant)	Kidney disorder	GLikely benign
Select item 1294548	NM_004998.4(MYO1E):c.*14C>G	MYO1E	Single nucleotide variant (3 prime UTR variant)	not provided +1 more	GBenign/Likely benign
Select item 403214	NM_004998.4(MYO1E):c.1593C>G (p.Ile531Met)	MYO1E (I531M)	Single nucleotide variant (missense variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 718354	NM_004998.4(MYO1E):c.1449G>A (p.Gln483=)	MYO1E	Single nucleotide variant (synonymous variant)	Kidney disorder +1 more	GBenign/Likely benign
Select item 1168375	NM_004998.4(MYO1E):c.1440G>A (p.Thr480=)	MYO1E	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 720699	NM_004998.4(MYO1E):c.643-4C>T	MYO1E	Single nucleotide variant (intron variant)	Kidney disorder +2 more	GBenign/Likely benign

ClinVar