"PreventionGenetics, part of Exact Sciences"[submitter] AND "APOC4-APO - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 329453	NM_000483.5(APOC2):c.-2C>T	APOC2, APOC4-APOC2	Single nucleotide variant (non-coding transcript variant +1 more)	Cardiovascular phenotype +3 more	GBenign/Likely benign
Select item 2581	NM_000483.5(APOC2):c.122A>C (p.Lys41Thr)	APOC2, APOC4-APOC2 (K41T)	Single nucleotide variant (non-coding transcript variant +1 more)	Cardiovascular phenotype +3 more	GConflicting classifications of pathogenicity
Select item 1776786	NM_000483.5(APOC2):c.162C>T (p.Ala54=)	APOC2, APOC4-APOC2	Single nucleotide variant (non-coding transcript variant +1 more)	APOC2-related disorder +1 more	GLikely benign
Select item 3043416	NM_000483.5(APOC2):c.*9C>T	APOC2, APOC4-APOC2	Single nucleotide variant (non-coding transcript variant +1 more)	APOC2-related disorder	GLikely benign

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