"MAGEA11-related disorder"[Disease/phenotype] AND "PreventionGenetics, - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3049970	NM_005366.5(MAGEA11):c.267-5C>T	MAGEA11	Single nucleotide variant (intron variant)	MAGEA11-related disorder	GLikely benign
Select item 3044833	NM_005366.5(MAGEA11):c.573C>A (p.Ser191Arg)	MAGEA11 (S162R +1 more)	Single nucleotide variant (missense variant)	MAGEA11-related disorder	GLikely benign
Select item 3034896	NM_005366.5(MAGEA11):c.900T>C (p.Asp300=)	MAGEA11	Single nucleotide variant (synonymous variant)	MAGEA11-related disorder	GLikely benign

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