"Ambry Genetics"[submitter] AND "LMO7-AS1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2410517	NM_005358.5(LMO7):c.53A>G (p.Tyr18Cys)	LMO7, LMO7-AS1 (Y18C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2211229	NM_005358.5(LMO7):c.112T>C (p.Cys38Arg)	LMO7-AS1, LMO7 (C38R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2602102	NM_005358.5(LMO7):c.156C>A (p.Asp52Glu)	LMO7, LMO7-AS1 (D52E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2537888	NM_005358.5(LMO7):c.169A>G (p.Lys57Glu)	LMO7, LMO7-AS1 (K57E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2523858	NM_005358.5(LMO7):c.179T>C (p.Ile60Thr)	LMO7, LMO7-AS1 (I60T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2490337	NM_005358.5(LMO7):c.214A>T (p.Ile72Phe)	LMO7, LMO7-AS1 (I72F)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

ClinVar