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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2628289	NM_007315.4(STAT1):c.2239-153A>C	STAT1	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 1264267	NM_007315.4(STAT1):c.2136-318G>A	STAT1	Single nucleotide variant (intron variant)	not specified +1 more	GBenign
Select item 333264	NM_007315.4(STAT1):c.1874-8C>T	STAT1	Single nucleotide variant (intron variant)	not specified +3 more	GBenign
Select item 1226208	NM_007315.4(STAT1):c.1728-103T>C	STAT1	Single nucleotide variant (intron variant)	not specified +1 more	GBenign
Select item 1250308	NM_007315.4(STAT1):c.1446+56A>G	STAT1	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 2628270	NM_007315.4(STAT1):c.1221+95G>A	STAT1	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 1280083	NM_007315.4(STAT1):c.1038-23A>G	STAT1	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 2628271	NM_007315.4(STAT1):c.633+42A>G	STAT1	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 1244456	NM_007315.4(STAT1):c.-1-305G>A	STAT1	Single nucleotide variant (intron variant)	not specified +1 more	GBenign

ClinVar