List of variants in gene combination APOB, LOC106560211 reported as uncertain significance by Robarts Research Institute, Western University

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_000384.3(APOB):c.218C>A (p.Ala73Asp)	rs377171241	0.00003
NM_000384.3(APOB):c.122-6C>T	rs1206711447
NM_000384.3(APOB):c.35_41del (p.Leu12fs)	rs1553301471
NM_000384.3(APOB):c.37_42del (p.Ala13_Leu14del)	rs1553301469
NM_000384.3(APOB):c.42_43del (p.Pro15fs)	rs1553301466
NM_000384.3(APOB):c.42del (p.Pro15fs)	rs1553301468

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