C0406740[trait identifier] AND "Baylor Genetics"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 663148	NM_024589.3(ROGDI):c.859T>C (p.Phe287Leu)	ROGDI (F287L)	Single nucleotide variant (missense variant +1 more)	Amelocerebrohypohidrotic syndrome +1 more	GUncertain significance
Select item 1032177	NM_024589.3(ROGDI):c.254C>T (p.Ala85Val)	ROGDI (A85V)	Single nucleotide variant (missense variant)	Amelocerebrohypohidrotic syndrome	GUncertain significance