"Clinical Genetics, Academic Medical Center"[submitter] AND "APOA1-AS" - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 734624	NM_000039.3(APOA1):c.327G>A (p.Glu109=)	APOA1, APOA1-AS	Single nucleotide variant (synonymous variant)	not provided +2 more	GLikely benign
Select item 302511	NM_000039.3(APOA1):c.9T>C (p.Ala3=)	APOA1, APOA1-AS	Single nucleotide variant (synonymous variant)	Hypoalphalipoproteinemia, primary, 2 +5 more	GBenign/Likely benign