List of variants in gene combination APOC2, APOC4-APOC2 reported as likely pathogenic for familial apolipoprotein C-II deficiency

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000483.5(APOC2):c.10C>T (p.Arg4Ter)	rs202190413
NM_000483.5(APOC2):c.189C>A (p.Tyr63Ter)	rs754423238
NM_000483.5(APOC2):c.274dup (p.Gln92fs)	rs756916028
NM_000483.5(APOC2):c.79C>T (p.Gln27Ter)

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