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Gene entry

ZNF469

zinc finger protein 469

Chromosome
16
Cytoband
16q24.2
Variants (rsID)
42

ZNF469 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 16 (region 16q24.2). Its official name is “zinc finger protein 469”. The reference table lists 42 variants (rsID) for this gene.

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Clinically classified variants

29 reference-table entries with clinical significance.

  • rs11640794Benignsingle nucleotide variantBrittle cornea syndrome 1
  • rs181785233Benignsingle nucleotide variantBrittle cornea syndrome 1|Ehlers-Danlos syndrome
  • rs184583062Benignsingle nucleotide variantBrittle cornea syndrome 1|Ehlers-Danlos syndrome
  • rs3812955Benignsingle nucleotide variantBrittle cornea syndrome 1|Ehlers-Danlos syndrome
  • rs45504291Benignsingle nucleotide variantBrittle cornea syndrome 1
  • rs75288466Benignsingle nucleotide variantEhlers-Danlos syndrome
  • rs116213189Conflicting interpretationssingle nucleotide variantBrittle cornea syndrome 1
  • rs144986357Conflicting interpretationssingle nucleotide variantBrittle cornea syndrome 1
  • rs145158875Conflicting interpretationssingle nucleotide variantBrittle cornea syndrome 1
  • rs148616993Conflicting interpretationssingle nucleotide variantBrittle cornea syndrome 1|Ehlers-Danlos syndrome
  • rs182269913Conflicting interpretationssingle nucleotide variantBrittle cornea syndrome 1|Ehlers-Danlos syndrome
  • rs184374078Conflicting interpretationssingle nucleotide variantBrittle cornea syndrome 1|Ehlers-Danlos syndrome
  • rs184894059Conflicting interpretationssingle nucleotide variantBrittle cornea syndrome 1
  • rs189476639Conflicting interpretationssingle nucleotide variantBrittle cornea syndrome 1|Ehlers-Danlos syndrome
  • rs199610834Conflicting interpretationssingle nucleotide variantBrittle cornea syndrome 1|Ehlers-Danlos syndrome
  • rs200153921Conflicting interpretationssingle nucleotide variantBrittle cornea syndrome 1|Ehlers-Danlos syndrome
  • rs273585618Conflicting interpretationssingle nucleotide variantKeratoconus 1|Brittle cornea syndrome 1
  • rs273585633Conflicting interpretationssingle nucleotide variantKeratoconus 1|Brittle cornea syndrome 1|Ehlers-Danlos syndrome
  • rs371897217Conflicting interpretationssingle nucleotide variantBrittle cornea syndrome 1|Ehlers-Danlos syndrome
  • rs373162171Conflicting interpretationssingle nucleotide variantBrittle cornea syndrome 1
  • rs56236932Conflicting interpretationssingle nucleotide variantBrittle cornea syndrome 1|Ehlers-Danlos syndrome
  • rs562559927Conflicting interpretationssingle nucleotide variantBrittle cornea syndrome 1
  • rs74547407Conflicting interpretationssingle nucleotide variantBrittle cornea syndrome 1
  • rs764487066Conflicting interpretationssingle nucleotide variantBrittle cornea syndrome 1|Ehlers-Danlos syndrome
  • rs768864900Conflicting interpretationssingle nucleotide variantBrittle cornea syndrome 1
  • rs775513309Conflicting interpretationssingle nucleotide variantBrittle cornea syndrome 1|Ehlers-Danlos syndrome
  • rs273585626Uncertain significancesingle nucleotide variantKeratoconus 1
  • rs281865151Uncertain significancesingle nucleotide variantKeratoconus 1
  • rs75706884Uncertain significancesingle nucleotide variantBrittle cornea syndrome 1

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.