C4479539[trait identifier] AND "Baylor Genetics"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1032441	NM_139284.3(LGI4):c.493C>T (p.Arg165Cys)	LGI4 (R165C)	Single nucleotide variant (missense variant)	Arthrogryposis multiplex congenita 1, neurogenic, with myelin defect	GUncertain significance
Select item 1032440	NM_139284.3(LGI4):c.17T>A (p.Ile6Asn)	LGI4 (I6N)	Single nucleotide variant (missense variant)	Arthrogryposis multiplex congenita 1, neurogenic, with myelin defect	GUncertain significance