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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1236007	NM_006567.5(FARS2):c.772+24C>T	FARS2	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 137292	NM_006567.5(FARS2):c.839A>G (p.Asn280Ser)	FARS2 (N280S +1 more)	Single nucleotide variant (missense variant +1 more)	Combined oxidative phosphorylation defect type 14 +2 more	GBenign
Select item 3256857	NM_006567.5(FARS2):c.904+555A>G	FARS2	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 3256845	NM_006567.5(FARS2):c.904+14334C>T	FARS2	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 1240596	NM_006567.5(FARS2):c.1065+81C>T	FARS2	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 3256817	NM_006567.5(FARS2):c.1217+6135A>G	FARS2	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 3256802	NM_006567.5(FARS2):c.1217+37690T>C	FARS2	Single nucleotide variant (intron variant)	not specified	GBenign

ClinVar