"Ambry Genetics"[submitter] AND "LOC130063466"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2486526	NM_031917.3(ANGPTL6):c.493C>T (p.Arg165Cys)	ANGPTL6, LOC130063466 (R165C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2352542	NM_031917.3(ANGPTL6):c.446A>C (p.Glu149Ala)	ANGPTL6, LOC130063466 (E149A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2243242	NM_031917.3(ANGPTL6):c.439T>C (p.Ser147Pro)	ANGPTL6, LOC130063466 (S147P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3118797	NM_031917.3(ANGPTL6):c.404C>A (p.Ala135Glu)	ANGPTL6, LOC130063466 (A135E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2593837	NM_031917.3(ANGPTL6):c.382C>G (p.Leu128Val)	ANGPTL6, LOC130063466 (L128V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2224250	NM_031917.3(ANGPTL6):c.371C>T (p.Pro124Leu)	ANGPTL6, LOC130063466 (P124L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar