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

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_000384.3(APOB):c.13651T>C (p.Tyr4551His)	rs145832414	0.00029
NM_000384.3(APOB):c.13670G>C (p.Gly4557Ala)	rs146687572	0.00008
NM_000384.3(APOB):c.13586A>G (p.His4529Arg)	rs958014928	0.00003
NM_000384.3(APOB):c.13600T>A (p.Tyr4534Asn)	rs1350773223	0.00001
NM_000384.3(APOB):c.13642A>G (p.Met4548Val)	rs1160435341
NM_000384.3(APOB):c.13648C>A (p.Pro4550Thr)	rs1191443988
NM_000384.3(APOB):c.13672G>A (p.Glu4558Lys)	rs1662980631
NM_000384.3(APOB):c.13678A>G (p.Thr4560Ala)	rs1662980568

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