"Ambry Genetics"[submitter] AND "LOC129388452"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3118877	NM_021146.4(ANGPTL7):c.691C>T (p.Arg231Cys)	ANGPTL7, LOC129388452 +1 more (R231C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3118880	NM_021146.4(ANGPTL7):c.811T>A (p.Phe271Ile)	ANGPTL7, LOC129388452 +1 more (F271I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3294286	NM_021146.4(ANGPTL7):c.818C>T (p.Thr273Ile)	ANGPTL7, LOC129388452 +1 more (T273I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3118885	NM_021146.4(ANGPTL7):c.863T>A (p.Leu288His)	ANGPTL7, LOC129388452 +1 more (L288H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2591576	NM_021146.4(ANGPTL7):c.865C>T (p.Arg289Cys)	ANGPTL7, LOC129388452 +1 more (R289C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2337180	NM_021146.4(ANGPTL7):c.869A>G (p.Lys290Arg)	ANGPTL7, LOC129388452 +1 more (K290R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

ClinVar