"Unidad de Genómica Garrahan, Hospital de Pediatría Garrahan"[submitte - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2628220	NM_001039569.2(AP1S3):c.429+78dup	AP1S3	Duplication (intron variant)	not specified	GBenign
Select item 2688202	NM_001039569.2(AP1S3):c.429+51_429+56dup	AP1S3	Duplication (intron variant)	not specified	GBenign
Select item 2628211	NM_001039569.2(AP1S3):c.429+33ATG[8]	AP1S3	Microsatellite (intron variant)	not specified	GBenign
Select item 2628169	NM_001039569.2(AP1S3):c.429+33ATG[9]	AP1S3	Microsatellite (intron variant)	not specified	GBenign
Select item 2628198	NM_001039569.2(AP1S3):c.291+2651T>C	AP1S3	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 2628237	NM_001039569.2(AP1S3):c.183-78_183-77insTT	AP1S3	Insertion (intron variant)	not specified	GBenign
Select item 2628301	NM_001039569.2(AP1S3):c.183-137G>A	AP1S3	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 2688467	NM_001039569.2(AP1S3):c.183-170A>G	AP1S3	Single nucleotide variant (intron variant)	not specified	GBenign

ClinVar