Neurodegeneration with ataxia and late-onset optic atrophy: genes and variants

Neurodegeneration with ataxia and late-onset optic atrophy is linked to 1 analyzed protein (SDHA). 5 DNA variants are known to cause it; 57 more are uncertain, and 0 of those already look disease-causing on computable evidence.

Last updated 2026-09-30. Research information, not medical advice.

Genes linked to Neurodegeneration with ataxia and late-onset optic atrophy

Known disease-causing variants in Neurodegeneration with ataxia and late-onset optic atrophy

VariantPositionProtein partClinical label
SDHA R554W554Disease-causing (★★)
SDHA R585W585Disease-causing (★★)
SDHA M1R1Disease-causing (★★)
SDHA M1L1Disease-causing (★★)
SDHA G260R260Disease-causing (★★)

Same protein, different disease

Diseases related to Neurodegeneration with ataxia and late-onset optic atrophy

Frequently asked questions

Which genes are linked to Neurodegeneration with ataxia and late-onset optic atrophy?

In CATVariant, Neurodegeneration with ataxia and late-onset optic atrophy is linked to 1 analyzed protein: SDHA (Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial).

How many genetic variants are linked to Neurodegeneration with ataxia and late-onset optic atrophy?

69 variants: 5 are classified as disease-causing (pathogenic or likely pathogenic) in ClinVar and 57 are of uncertain significance or have conflicting reports.

Which uncertain variants in Neurodegeneration with ataxia and late-onset optic atrophy look disease-causing?

None of the uncertain variants currently reaches the likely-pathogenic range on computable evidence alone.

About this data

Variant–disease links come from ClinVar, Open Targets and UniProt, pooled from the latest public CATVariant analysis of each human protein. Evidence scores use the ACMG/AMP Bayesian points scale with computable criteria only (position among known disease variants, rarity in gnomAD, calibrated predictors, deep mutational scanning); there is no family or patient data, so they prioritise variants for expert review and never classify them.

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