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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 13985	NM_016816.4(OAS1):c.484G>A (p.Gly162Ser)	OAS1 (G162S)	Single nucleotide variant (missense variant)	not specified +1 more	GBenign
Select item 1156518	NM_016816.4(OAS1):c.1039-1G>A	OAS1	Single nucleotide variant (3 prime UTR variant +3 more)	not specified +1 more	GBenign/Likely benign
Select item 1167216	NM_016816.4(OAS1):c.1054G>A (p.Ala352Thr)	OAS1 (A352T)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign
Select item 1168534	NM_016816.4(OAS1):c.1082G>C (p.Arg361Thr)	OAS1 (R361T)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign
Select item 1246789	NM_016816.4(OAS1):c.*84G>A	OAS1 (G397R)	Single nucleotide variant (missense variant +2 more)	not specified +1 more	GBenign
Select item 2688063	NM_001320151.2(OAS1):c.1039-39C>T	OAS1	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 2687938	NM_001320151.2(OAS1):c.*32G>C	OAS1	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GBenign

ClinVar