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Gene entry

EDA

ectodysplasin A

Chromosome
X
Cytoband
Xq13.1
Variants (rsID)
72

EDA is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome X (region Xq13.1). Its official name is “ectodysplasin A”. The reference table lists 72 variants (rsID) for this gene.

Clinically classified variants

11 reference-table entries with clinical significance.

  • rs132630309Conflicting interpretationssingle nucleotide variantHypohidrotic X-linked ectodermal dysplasia
  • rs132630315Conflicting interpretationssingle nucleotide variantHypohidrotic X-linked ectodermal dysplasia
  • rs132630310Pathogenicsingle nucleotide variantHypohidrotic X-linked ectodermal dysplasia
  • rs132630311Pathogenicsingle nucleotide variantHypohidrotic X-linked ectodermal dysplasia
  • rs132630312Pathogenicsingle nucleotide variantHypohidrotic X-linked ectodermal dysplasia|Tooth agenesis, selective, X-linked, 1|Hypohidrotic X-linked ectodermal dysplasia
  • rs132630313Pathogenicsingle nucleotide variantHypohidrotic X-linked ectodermal dysplasia
  • rs132630314Pathogenicsingle nucleotide variantHypohidrotic X-linked ectodermal dysplasia
  • rs132630317Pathogenicsingle nucleotide variantHypohidrotic X-linked ectodermal dysplasia
  • rs132630319Pathogenicsingle nucleotide variantTooth agenesis, selective, X-linked, 1
  • rs132630320Pathogenicsingle nucleotide variantTooth agenesis, selective, X-linked, 1
  • rs132630321Pathogenicsingle nucleotide variantTooth agenesis, selective, X-linked, 1|Hypohidrotic X-linked ectodermal dysplasia

Other listed variants

Public references

Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.