"ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1005027	NM_031206.7(LAS1L):c.2051G>A (p.Arg684Gln)	LAS1L (R365Q +5 more)	Single nucleotide variant (missense variant +1 more)	Wilson-Turner syndrome +1 more	GUncertain significance
Select item 1170743	NM_031206.7(LAS1L):c.1341A>G (p.Ala447=)	LAS1L	Single nucleotide variant (synonymous variant +1 more)	Wilson-Turner syndrome	GBenign/Likely benign