ClinVar for MedGen (Select 902781) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 786064	NM_004134.7(HSPA9):c.21T>G (p.Ala7=)	HSPA9	Single nucleotide variant (synonymous variant)	Autosomal dominant sideroblastic anemia +2 more	GBenign/Likely benign
Select item 224070	NM_004134.7(HSPA9):c.1373_1378del (p.Ile458_Asn459del)	HSPA9	Deletion (inframe_deletion)	not provided	GUncertain significance
Select item 224069	NM_004134.7(HSPA9):c.409_410del (p.Asp136_Ile137insTer)	HSPA9	Deletion (nonsense)	Autosomal dominant sideroblastic anemia	GPathogenic

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