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

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1283277	NM_001197104.2(KMT2A):c.4820-45T>C	KMT2A	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1187987	NM_001197104.2(KMT2A):c.5961+37del	KMT2A	Deletion (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 1288979	NM_001197104.2(KMT2A):c.11644-46G>A	KMT2A, TTC36-AS1	Single nucleotide variant (intron variant)	not specified +1 more	GBenign

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