"GeneDx"[submitter] AND "LOC126862485"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59583	GRCh38/hg38 17p13.1(chr17:7478195-8435524)x1	ALOX12B, ALOX15B +191 more	Copy number loss	See cases	GPathogenic
Select item 325982	NM_021628.3(ALOXE3):c.-300C>G	ALOXE3, LOC126862485 (P33A)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign
Select item 325983	NM_021628.3(ALOXE3):c.-304G>T	ALOXE3, LOC126862485 (Q31H)	Single nucleotide variant (missense variant +1 more)	Autosomal recessive congenital ichthyosis 3 +2 more	GBenign/Likely benign
Select item 1269386	NM_021628.3(ALOXE3):c.-313-78C>A	ALOXE3, LOC126862485	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1188973	NM_001165960.1(ALOXE3):c.32C>T (p.Pro11Leu)	ALOXE3, LOC126862485 (P11L)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 1278146	NM_001165960.1(ALOXE3):c.-43G>T	ALOXE3, LOC126862485	Single nucleotide variant (5 prime UTR variant)	not provided	GBenign

ClinVar