Variants in gene combination APOB, LOC106560211 with conflicting interpretations reported as "benign and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 3

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HGVS	dbSNP	gnomAD frequency
NM_000384.3(APOB):c.129G>C (p.Ala43=)	rs12720850	0.00580
NM_000384.3(APOB):c.26TGGCGCTGC[1] (p.9LAL[1])	rs17240441
NM_000384.3(APOB):c.49CTG[8] (p.Leu21_Leu22dup)	rs745520533

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