C5677030[trait identifier] AND "Genome-Nilou Lab"[submitter] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 302500	NM_000039.3(APOA1):c.*19C>G	APOA1	Single nucleotide variant (3 prime UTR variant)	Familial visceral amyloidosis, Ostertag type +4 more	GBenign
Select item 302501	NM_000039.3(APOA1):c.732C>G (p.Pro244=)	APOA1	Single nucleotide variant (synonymous variant)	Hypoalphalipoproteinemia, primary, 2 +6 more	GBenign/Likely benign
Select item 1217233	NM_000039.3(APOA1):c.564C>G (p.Ala188=)	APOA1	Single nucleotide variant (synonymous variant)	not provided +5 more	GBenign/Likely benign
Select item 1251605	NM_000039.3(APOA1):c.200+33T>C	APOA1, APOA1-AS	Single nucleotide variant (intron variant)	not provided +3 more	GBenign
Select item 302507	NM_000039.3(APOA1):c.181G>A (p.Ala61Thr)	APOA1, APOA1-AS (A61T)	Single nucleotide variant (missense variant)	Hypoalphalipoproteinemia, primary, 2 +6 more	GBenign
Select item 1225953	NM_000039.3(APOA1):c.43+41T>C	APOA1, APOA1-AS	Single nucleotide variant (intron variant)	not provided +3 more	GBenign
Select item 302511	NM_000039.3(APOA1):c.9T>C (p.Ala3=)	APOA1-AS, APOA1	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +5 more	GBenign/Likely benign

ClinVar