"PreventionGenetics, part of Exact Sciences"[submitter] AND "LOC126859 - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3050402	NM_014611.3(MDN1):c.15156C>T (p.Ala5052=)	LOC126859739, MDN1 +1 more	Single nucleotide variant (synonymous variant)	MDN1-related disorder	GLikely benign
Select item 3058944	NM_014611.3(MDN1):c.14970C>T (p.Ala4990=)	LOC126859739, MDN1 +1 more	Single nucleotide variant (synonymous variant)	MDN1-related disorder	GBenign
Select item 3045534	NM_014611.3(MDN1):c.14757T>G (p.Gly4919=)	LOC126859739, MDN1 +1 more	Single nucleotide variant (synonymous variant)	MDN1-related disorder	GBenign

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ClinVar