Variants in gene APOB with conflicting interpretations "likely benign" and "pathogenic"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (pathogenic) 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_000384.3(APOB):c.3337G>C (p.Asp1113His)	rs12713844	0.00735
NM_000384.3(APOB):c.8216C>T (p.Pro2739Leu)	rs676210

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