"GeneDx"[submitter] AND "MDN1"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58438	GRCh38/hg38 6q14.1-16.1(chr6:82569098-93753476)x1	AKIRIN2, ANKRD6 +220 more	Copy number loss	See cases	GPathogenic
Select item 1278999	NM_014611.3(MDN1):c.4086T>C (p.His1362=)	MDN1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1231787	NM_014611.3(MDN1):c.1318T>G (p.Phe440Val)	MDN1 (F440V)	Single nucleotide variant (missense variant)	not provided	GBenign

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