"GeneDx"[submitter] AND "GPX1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1236610	NC_000003.12:g.49357126dup	GPX1	Duplication	not provided	GBenign
Select item 16082	NM_000581.4(GPX1):c.599C>T (p.Pro200Leu)	GPX1 (P200L +1 more)	Single nucleotide variant (missense variant +1 more)	Gluthathione peroxidase deficiency +1 more	GBenign
Select item 1276107	NM_000581.4(GPX1):c.21GGC[4] (p.Ala12_Ala13del)	GPX1	Microsatellite (inframe_deletion)	not provided	GBenign
Select item 1230493	NM_000581.4(GPX1):c.21GGC[5] (p.Ala13del)	GPX1 (A13del)	Microsatellite (inframe_deletion)	not provided	GBenign
Select item 1252486	NM_000581.4(GPX1):c.-46C>T	GPX1	Single nucleotide variant (5 prime UTR variant)	not provided	GBenign
Select item 253356	GRCh37/hg19 3p22.2-21.31(chr3:37028313-49929220)x3	ABHD5, ACAA1 +177 more	Copy number gain	See cases	GLikely pathogenic

ClinVar