"PreventionGenetics, part of Exact Sciences"[submitter] AND "LOC108491 - ClinVar - NCBI

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Items: 3

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1187967	NM_001371904.1(APOA5):c.168G>A (p.Leu56=)	LOC108491825, APOA5	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +2 more	GLikely benign
Select item 1776373	NM_001371904.1(APOA5):c.161+3G>A	APOA5, LOC108491825	Single nucleotide variant (intron variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 1604153	NM_001371904.1(APOA5):c.70C>A (p.Arg24=)	APOA5, LOC108491825	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +2 more	GLikely benign

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