List of variants in gene APOB reported as uncertain significance 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_000384.3(APOB):c.11288T>C (p.Leu3763Pro)	rs1663106152	0.00001
NM_000384.3(APOB):c.10072A>C (p.Asn3358His)	rs1663155110
NM_000384.3(APOB):c.10147G>A (p.Gly3383Ser)	rs1663152041
NM_000384.3(APOB):c.10540G>A (p.Ala3514Thr)	rs747633151
NM_000384.3(APOB):c.13320del (p.Glu4441fs)	rs750076573
NM_000384.3(APOB):c.6047A>G (p.Asp2016Gly)
NM_000384.3(APOB):c.6592A>G (p.Ile2198Val)
NM_000384.3(APOB):c.9105T>A (p.Asn3035Lys)	rs147510760

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