"Ambry Genetics"[submitter] AND "LCN1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2226778	NM_002297.4(LCN1):c.233G>A (p.Arg78Gln)	LCN1 (R78Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2602790	NM_002297.4(LCN1):c.400G>A (p.Val134Met)	LCN1 (V134M)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2485179	NM_002297.4(LCN1):c.415A>G (p.Lys139Glu)	LCN1 (K139E)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2346060	NM_002297.4(LCN1):c.454G>A (p.Ala152Thr)	LCN1 (A152T)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2545896	NM_002297.4(LCN1):c.463C>T (p.Arg155Cys)	LCN1 (R155C)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2342000	NM_002297.4(LCN1):c.464G>A (p.Arg155His)	LCN1 (A151T +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2391596	NM_002297.4(LCN1):c.499C>G (p.Gln167Glu)	LCN1 (Q167E)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2326051	NM_002297.4(LCN1):c.526G>A (p.Asp176Asn)	LCN1 (D176N)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance

ClinVar