Spondyloepiphyseal dysplasia, Stanescu type: genes and variants

Spondyloepiphyseal dysplasia, Stanescu type is linked to 1 analyzed protein (COL2A1). 10 DNA variants are known to cause it; 0 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 Spondyloepiphyseal dysplasia, Stanescu type

Known disease-causing variants in Spondyloepiphyseal dysplasia, Stanescu type

VariantPositionProtein partClinical label
COL2A1 G723S723Triple-helical regionDisease-causing (★★)
COL2A1 G207R207Triple-helical regionDisease-causing (★★)
COL2A1 G516S516Triple-helical regionDisease-causing (★★)
COL2A1 G654S654Triple-helical regionDisease-causing (★★)
COL2A1 G1152R1152Triple-helical regionDisease-causing (★★)
COL2A1 G447S447Triple-helical regionDisease-causing (★★)
COL2A1 G1086R1086Triple-helical regionDisease-causing (★★)
COL2A1 G1188A1188Triple-helical regionDisease-causing (★)
COL2A1 P917L917Triple-helical regionDisease-causing (★)
COL2A1 G1176V1176Triple-helical regionDisease-causing (★)

Same protein, different disease

Diseases related to Spondyloepiphyseal dysplasia, Stanescu type

Frequently asked questions

Which genes are linked to Spondyloepiphyseal dysplasia, Stanescu type?

In CATVariant, Spondyloepiphyseal dysplasia, Stanescu type is linked to 1 analyzed protein: COL2A1 (Collagen alpha-1(II) chain).

How many genetic variants are linked to Spondyloepiphyseal dysplasia, Stanescu type?

19 variants: 10 are classified as disease-causing (pathogenic or likely pathogenic) in ClinVar and 0 are of uncertain significance or have conflicting reports.

Which uncertain variants in Spondyloepiphyseal dysplasia, Stanescu type 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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