"GeneDx"[submitter] AND "LOC106560211"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3343607	NM_000384.3(APOB):c.193C>T (p.Pro65Ser)	APOB, LOC106560211 (P65S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 517778	NM_000384.3(APOB):c.168T>C (p.Tyr56=)	APOB, LOC106560211	Single nucleotide variant (synonymous variant)	Familial hypercholesterolemia +4 more	GBenign/Likely benign
Select item 334189	NM_000384.3(APOB):c.129G>C (p.Ala43=)	APOB, LOC106560211	Single nucleotide variant (synonymous variant)	Hypercholesterolemia, autosomal dominant, type B +4 more	GBenign
Select item 682399	NM_000384.3(APOB):c.82+12G>C	APOB, LOC106560211	Single nucleotide variant (intron variant)	not provided +2 more	GLikely benign
Select item 426250	NM_000384.3(APOB):c.49CTG[8] (p.Leu21_Leu22dup)	APOB, LOC106560211	Microsatellite (inframe_insertion)	Familial hypercholesterolemia +4 more	GBenign/Likely benign
Select item 255983	NM_000384.3(APOB):c.26TGGCGCTGC[1] (p.9LAL[1])	APOB, LOC106560211	Microsatellite (inframe_deletion)	not specified +6 more	GBenign/Likely benign
Select item 2952375	NM_000384.3(APOB):c.18_27delinsT (p.9_11LAL[1])	APOB, LOC106560211	Indel (inframe_deletion)	not provided +2 more	GUncertain significance

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