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: 4

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HGVS	dbSNP
NM_000384.3(APOB):c.10739A>G (p.Asn3580Ser)	rs762028704
NM_000384.3(APOB):c.10780T>C (p.Trp3594Arg)
NM_000384.3(APOB):c.10808A>G (p.His3603Arg)	rs370481987
NM_000384.3(APOB):c.3337G>C (p.Asp1113His)

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