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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2331722	NM_002309.5(LIF):c.596C>T (p.Ala199Val)	LIF (A199V)	Single nucleotide variant (3 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2392770	NM_002309.5(LIF):c.475T>C (p.Tyr159His)	LIF (Y159H)	Single nucleotide variant (3 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2294575	NM_002309.5(LIF):c.421G>A (p.Ala141Thr)	LIF (A141T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2329062	NM_002309.5(LIF):c.226A>G (p.Asn76Asp)	LIF (N76D +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2493365	NM_002309.5(LIF):c.85C>T (p.Pro29Ser)	LIF (P29S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2598359	NM_002309.5(LIF):c.73C>T (p.Leu25Phe)	LIF (L25F)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance

ClinVar