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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 57808	GRCh38/hg38 14q24.3(chr14:73877072-78042422)x1	ABCD4, ACYP1 +227 more	Copy number loss	See cases	GPathogenic
Select item 1212397	NC_000014.9:g.74303027G>A	ABCD4, LOC130056092 +1 more	Single nucleotide variant (genic upstream transcript variant)	not provided	GLikely benign
Select item 1300480	NC_000014.9:g.74303033G>C	ABCD4, LOC130056092 +1 more	Single nucleotide variant (genic upstream transcript variant)	not provided	GLikely benign
Select item 1326415	NC_000014.9:g.74303036A>G	ABCD4, LOC130056092 +1 more	Single nucleotide variant (genic upstream transcript variant)	not provided	GLikely benign
Select item 1181620	NC_000014.9:g.74303138C>T	ABCD4, LOC130056092 +1 more	Single nucleotide variant	not provided	GBenign
Select item 1300997	NC_000014.9:g.74303196T>A	ABCD4, LOC130056092 +1 more	Single nucleotide variant	not provided	GLikely benign
Select item 1234864	NC_000014.9:g.74303274G>A	ABCD4, LOC130056092 +1 more	Single nucleotide variant	not provided	GBenign

ClinVar