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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2688187	NM_017553.3(INO80):c.4453+46A>C	INO80	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 2688065	NM_017553.3(INO80):c.4078-39C>T	INO80	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 2688291	NM_017553.3(INO80):c.3833-109A>C	INO80	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 2688066	NM_017553.3(INO80):c.3274+34G>C	INO80, INO80-AS1	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 2687940	NM_017553.3(INO80):c.2274+35A>G	INO80	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 2688243	NM_017553.3(INO80):c.2071-96C>T	INO80	Single nucleotide variant (intron variant)	not specified	GBenign

ClinVar