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

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59821	GRCh38/hg38 12q24.21-24.33(chr12:115131583-133166920)x3	LOC130009192, LOC130009193 +892 more	Copy number gain	See cases	GPathogenic
Select item 57609	GRCh38/hg38 12q24.31(chr12:120504068-122459718)x1	ACADS, ANAPC5 +175 more	Copy number loss	See cases	GPathogenic
Select item 1227142	NM_014730.4(MLEC):c.236-2968C>T	MLEC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1237132	NM_014730.4(MLEC):c.414+28C>T	MLEC	Single nucleotide variant (intron variant)	not provided	GBenign

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