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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 138864	NM_002872.5(RAC2):c.477T>C (p.Ala159=)	RAC2	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign
Select item 2688324	NM_002872.5(RAC2):c.449-1206A>G	RAC2	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 1327931	NM_002872.5(RAC2):c.448+37A>G	LOC130067355, RAC2	Single nucleotide variant (intron variant)	not specified +3 more	GBenign
Select item 1327932	NM_002872.5(RAC2):c.448+25C>G	LOC130067355, RAC2	Single nucleotide variant (intron variant)	Immunodeficiency 73c with defective neutrophil chemotaxis and hypogammaglobulinemia +3 more	GBenign
Select item 1164430	NM_002872.5(RAC2):c.226-21dup	RAC2	Duplication (intron variant)	not provided +4 more	GBenign
Select item 2688287	NM_002872.5(RAC2):c.226-111T>C	RAC2	Single nucleotide variant (intron variant)	not specified	GBenign

ClinVar