"Ambry Genetics"[submitter] AND "LXN"[gene] - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2304393	NM_020169.4(LXN):c.560T>C (p.Ile187Thr)	GFM1, LXN (I187T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2237417	NM_020169.4(LXN):c.391C>G (p.Pro131Ala)	GFM1, LXN (P131A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2463612	NM_020169.4(LXN):c.80C>T (p.Thr27Ile)	GFM1, LXN (T27I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2324480	NM_020169.4(LXN):c.52C>G (p.Gln18Glu)	GFM1, LXN (Q18E)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign

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