ClinVar for MedGen (Select 330802) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3064723	NM_001319206.4(MEF2A):c.407A>G (p.Gln136Arg)	MEF2A (Q136R +6 more)	Single nucleotide variant (missense variant +1 more)	Coronary artery disease, autosomal dominant, 1	GUncertain significance
Select item 778574	NM_001319206.4(MEF2A):c.1253AGC[13] (p.Gln427_Gln428dup)	MEF2A	Microsatellite (inframe_insertion)	not provided +1 more	GBenign
Select item 8948	NM_001319206.4(MEF2A):c.1313_1333del (p.Gln438_Pro444del)	MEF2A	Deletion (inframe_deletion)	Coronary artery disease, autosomal dominant, 1	GPathogenic

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