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

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2688018	NM_003120.3(SPI1):c.493+334T>G	SPI1	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 2688186	NM_003120.3(SPI1):c.493+105TG[8]	SPI1	Microsatellite (intron variant)	not specified	GBenign
Select item 2687986	NM_003120.3(SPI1):c.493+55C>A	SPI1	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 2687976	NM_003120.3(SPI1):c.331-36C>T	SPI1	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 2688056	NM_003120.3(SPI1):c.46-73C>T	SPI1	Single nucleotide variant (intron variant)	not specified	GBenign

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