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Gene entry

ALDH3A2

aldehyde dehydrogenase 3 family member A2

Chromosome
17
Cytoband
17p11.2
Variants (rsID)
16

ALDH3A2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 17 (region 17p11.2). Its official name is “aldehyde dehydrogenase 3 family member A2”. The reference table lists 16 variants (rsID) for this gene.

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Clinically classified variants

5 reference-table entries with clinical significance.

  • rs72547561Pathogenicsingle nucleotide variantSjögren-Larsson syndrome
  • rs72547562Pathogenicsingle nucleotide variantSjögren-Larsson syndrome
  • rs72547569Pathogenicsingle nucleotide variantSjögren-Larsson syndrome
  • rs72547571Pathogenicsingle nucleotide variantSjögren-Larsson syndrome
  • rs72547575Pathogenicsingle nucleotide variantSjögren-Larsson syndrome

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.