"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 2688421	NM_001561.6(TNFRSF9):c.680-1051A>G	TNFRSF9	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 2688461	NM_001561.6(TNFRSF9):c.413+1248GTTT[7]	TNFRSF9	Microsatellite (intron variant)	not specified	GBenign
Select item 2688454	NM_001561.6(TNFRSF9):c.413+1116T>C	TNFRSF9	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 2688134	NM_001561.6(TNFRSF9):c.101-75A>C	TNFRSF9	Single nucleotide variant (intron variant)	not specified	GBenign

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