List of variants in gene combination APOB, APOB3'MAR reported as likely benign for Familial hypercholesterolemia

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000384.3(APOB):c.13680T>C (p.Thr4560=)	rs72654427	0.00064
NM_000384.3(APOB):c.13608G>T (p.Thr4536=)	rs377641527
NM_000384.3(APOB):c.13638A>C (p.Thr4546=)	rs777726812

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