Related gene-specific medical variations for Gene (Select 345) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2582727	NM_000040.3(APOC3):c.91T>G (p.Phe31Val)	APOC3 (F31V)	Single nucleotide variant (missense variant)	Apolipoprotein c-III deficiency	GUncertain significance
Select item 1803900	NM_000040.3(APOC3):c.161A>G (p.Gln54Arg)	APOC3 (Q54R)	Single nucleotide variant (missense variant)	Apolipoprotein c-III deficiency	GUncertain significance
Select item 1803817	NM_000040.3(APOC3):c.148G>A (p.Val50Met)	APOC3 (V50M)	Single nucleotide variant (missense variant)	Apolipoprotein c-III deficiency	GUncertain significance

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