Related gene-specific medical variations for Gene (Select 51218) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2432168	NM_016417.3(GLRX5):c.425G>A (p.Gly142Glu)	GLRX5 (G142E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1252035	NM_016417.3(GLRX5):c.197A>C (p.Gln66Pro)	GLRX5 (Q66P)	Single nucleotide variant (missense variant)	Spasticity-ataxia-gait anomalies syndrome	GPathogenic
Select item 156435	NM_016417.3(GLRX5):c.129G>C (p.Glu43Asp)	GLRX5 (E43D)	Single nucleotide variant (missense variant)	not provided	Gnot provided

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