Gene entry
DUOX2
dual oxidase 2
- Chromosome
- 15
- Cytoband
- 15q21.1
- Variants (rsID)
- 33
DUOX2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 15 (region 15q21.1). Its official name is “dual oxidase 2”. The reference table lists 33 variants (rsID) for this gene.
Clinically classified variants
13 reference-table entries with clinical significance.
- rs138353181Benignsingle nucleotide variantThyroid dyshormonogenesis 6|Meckel syndrome, type 11
- rs2001616Benignsingle nucleotide variantThyroid dyshormonogenesis 6
- rs269868Benignsingle nucleotide variantThyroid dyshormonogenesis 6
- rs57659670Benignsingle nucleotide variantThyroid dyshormonogenesis 6
- rs79393107Benignsingle nucleotide variantThyroid dyshormonogenesis 6
- rs143471358Conflicting interpretationssingle nucleotide variantThyroid dyshormonogenesis 6
- rs181461079Conflicting interpretationssingle nucleotide variantNongoitrous Euthyroid Hyperthyrotropinemia|Thyroid dyshormonogenesis 6
- rs199589510Conflicting interpretationssingle nucleotide variantThyroid dyshormonogenesis 6
- rs369394906Conflicting interpretationssingle nucleotide variantThyroid dyshormonogenesis 6
- rs199752932Likely pathogenicsingle nucleotide variantThyroid dyshormonogenesis 6
- rs119472029Pathogenicsingle nucleotide variantThyroid dyshormonogenesis 6
- rs530719719PathogenicDeletionFamilial thyroid dyshormonogenesis|Congenital hypothyroidism|Nongoitrous Euthyroid Hyperthyrotropinemia|Inborn genetic diseases|Thyroid dyshormonogenesis 6
- rs144543420Uncertain significancesingle nucleotide variant
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.