"Genome-Nilou Lab"[submitter] AND "APOB"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 128418	NM_000384.3(APOB):c.13013G>A (p.Ser4338Asn)	APOB (S4338N)	Single nucleotide variant (missense variant)	Hypercholesterolemia, familial, 1 +6 more	GBenign
Select item 128417	NM_000384.3(APOB):c.12541G>A (p.Glu4181Lys)	APOB (E4181K)	Single nucleotide variant (missense variant)	not specified +6 more	GBenign/Likely benign
Select item 128425	NM_000384.3(APOB):c.7545C>T (p.Thr2515=)	APOB	Single nucleotide variant (synonymous variant)	Hypercholesterolemia, familial, 1 +6 more	GBenign
Select item 1169879	NM_000384.3(APOB):c.6936C>T (p.Asp2312=)	APOB	Single nucleotide variant (synonymous variant)	not provided +4 more	GBenign
Select item 1192327	NM_000384.3(APOB):c.3843-77T>C	APOB	Single nucleotide variant (intron variant)	Familial hypobetalipoproteinemia 1 +2 more	GBenign
Select item 128420	NM_000384.3(APOB):c.1853C>T (p.Ala618Val)	APOB (A618V)	Single nucleotide variant (missense variant)	not specified +6 more	GBenign/Likely benign
Select item 128422	NM_000384.3(APOB):c.293C>T (p.Thr98Ile)	APOB (T98I)	Single nucleotide variant (missense variant)	Hypercholesterolemia, familial, 1 +6 more	GBenign/Likely benign
Select item 1192328	NM_000384.3(APOB):c.237+92G>T	APOB, LOC106560211	Single nucleotide variant (intron variant)	not provided +2 more	GBenign

ClinVar