C5231558[trait identifier] AND "Fulgent Genetics, Fulgent Genetics"[su - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 364391	NM_005502.4(ABCA1):c.5383-20_5383-18dup	ABCA1	Duplication (intron variant)	Familial High Density Lipoprotein Deficiency +4 more	GBenign
Select item 496293	NM_005502.4(ABCA1):c.2961-10C>T	ABCA1	Single nucleotide variant (intron variant)	not provided +2 more	GBenign/Likely benign
Select item 496292	NM_005502.4(ABCA1):c.2868C>T (p.Thr956=)	ABCA1	Single nucleotide variant (synonymous variant)	Hypoalphalipoproteinemia, primary, 1 +3 more	GBenign/Likely benign
Select item 974983	NM_005502.4(ABCA1):c.2338-17T>C	ABCA1	Single nucleotide variant (intron variant)	not provided +3 more	GBenign/Likely benign
Select item 364453	NM_005502.4(ABCA1):c.814-14dup	ABCA1	Duplication (intron variant)	not specified +4 more	GBenign
Select item 302508	NM_000039.3(APOA1):c.168G>A (p.Gln56=)	APOA1, APOA1-AS	Single nucleotide variant (synonymous variant)	Familial visceral amyloidosis, Ostertag type +5 more	GConflicting classifications of pathogenicity

ClinVar