"PreventionGenetics, part of Exact Sciences"[submitter] AND "APOA2"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 496142	NM_001643.2(APOA2):c.288G>A (p.Gln96=)	APOA2	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 293292	NM_001643.2(APOA2):c.186-4C>T	APOA2	Single nucleotide variant (intron variant)	Apolipoprotein A-II deficiency +1 more	GBenign
Select item 3046168	NM_001643.2(APOA2):c.53-43TG[11]	APOA2	Microsatellite (intron variant)	APOA2-related disorder	GLikely benign
Select item 933213	NM_001643.2(APOA2):c.53-43TG[18]	APOA2	Microsatellite (intron variant)	APOA2-related disorder +1 more	GBenign
Select item 929172	NM_001643.2(APOA2):c.53-43TG[14]	APOA2	Microsatellite (intron variant)	not specified +1 more	GBenign
Select item 293295	NM_001643.2(APOA2):c.53-43TG[16]	APOA2	Microsatellite (intron variant)	Apolipoprotein A-II deficiency +2 more	GConflicting classifications of pathogenicity

ClinVar