"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 2688272	NM_000269.3(NME1):c.-5+600C>G	NME1, NME1-NME2	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GBenign
Select item 2688150	NM_000269.3(NME1):c.-5+604G>A	NME1, NME1-NME2	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GBenign
Select item 2688180	NM_000269.3(NME1):c.342-53C>A	NME1, NME1-NME2	Single nucleotide variant (intron variant)	not specified	GBenign

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