McCune-Albright syndrome: genes and variants

McCune-Albright syndrome is linked to 1 analyzed protein (GNAS). 5 DNA variants are known to cause it; 3 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 McCune-Albright syndrome

Known disease-causing variants in McCune-Albright syndrome

VariantPositionProtein partClinical label
GNAS R201C201G-alphaDisease-causing (★★)
GNAS M1V1Disease-causing (★★)
GNAS Q227R227G-alphaDisease-causing (★)
GNAS Q213R213G-alphaDisease-causing (★)
GNAS R201G201G-alphaDisease-causing

Same protein, different disease

Diseases related to McCune-Albright syndrome

Frequently asked questions

Which genes are linked to McCune-Albright syndrome?

In CATVariant, McCune-Albright syndrome is linked to 1 analyzed protein: GNAS (Guanine nucleotide-binding protein G(s) subunit alpha isoforms short).

How many genetic variants are linked to McCune-Albright syndrome?

22 variants: 5 are classified as disease-causing (pathogenic or likely pathogenic) in ClinVar and 3 are of uncertain significance or have conflicting reports.

Which uncertain variants in McCune-Albright syndrome 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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