"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "APOA1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2137255	NM_000039.3(APOA1):c.590G>C (p.Arg197Pro)	APOA1 (R88P +1 more)	Single nucleotide variant (missense variant)	not provided	GPathogenic
Select item 1163526	NM_000039.3(APOA1):c.455A>G (p.Glu152Gly)	APOA1, APOA1-AS (E152G +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GUncertain significance
Select item 636899	NM_000039.3(APOA1):c.388AAG[1] (p.Lys131del)	APOA1, APOA1-AS (K131del +1 more)	Microsatellite (inframe_deletion +2 more)	Chronic kidney disease +4 more	GConflicting classifications of pathogenicity
Select item 1163527	NM_000039.3(APOA1):c.296T>C (p.Leu99Pro)	APOA1, APOA1-AS (L99P)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GPathogenic/Likely pathogenic
Select item 2174166	NM_000039.3(APOA1):c.227G>A (p.Ser76Asn)	APOA1-AS, APOA1 (S76N)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 17920	NM_000039.3(APOA1):c.101G>T (p.Arg34Leu)	APOA1, APOA1-AS (R34L)	Single nucleotide variant (missense variant)	Hypoalphalipoproteinemia, primary, 2 +3 more	GUncertain significance

ClinVar