"Fulgent Genetics, Fulgent Genetics"[submitter] AND "LOC106560211"[gen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 548044	NM_000384.3(APOB):c.218C>A (p.Ala73Asp)	APOB, LOC106560211 (A73D)	Single nucleotide variant (missense variant)	Hypercholesterolemia, autosomal dominant, type B +5 more	GConflicting classifications of pathogenicity
Select item 920621	NM_000384.3(APOB):c.187G>A (p.Gly63Arg)	APOB, LOC106560211 (G63R)	Single nucleotide variant (missense variant)	Familial hypercholesterolemia +3 more	GUncertain significance
Select item 921121	NM_000384.3(APOB):c.166T>C (p.Tyr56His)	APOB, LOC106560211 (Y56H)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +3 more	GConflicting classifications of pathogenicity
Select item 431490	NM_000384.3(APOB):c.154T>C (p.Tyr52His)	APOB, LOC106560211 (Y52H)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +5 more	GUncertain significance
Select item 697560	NM_000384.3(APOB):c.81C>G (p.Ala27=)	APOB, LOC106560211	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +2 more	GLikely benign
Select item 1115315	NM_000384.3(APOB):c.36G>T (p.Leu12=)	APOB, LOC106560211	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +2 more	GLikely benign
Select item 897863	NM_000384.3(APOB):c.35T>C (p.Leu12Pro)	APOB, LOC106560211 (L12P)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance

ClinVar