Related gene-specific medical variations for Gene (Select 79697) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3154479	NM_024644.5(RIOX1):c.80G>A (p.Gly27Glu)	ACOT1, HEATR4 +1 more (G27E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 788892	NM_024644.5(RIOX1):c.1587C>G (p.Arg529=)	RIOX1, ACOT1 +1 more	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign/Likely benign
Select item 768664	NM_024644.5(RIOX1):c.94C>A (p.Leu32Met)	HEATR4, RIOX1 +1 more (L32M)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign

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