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Gene entry

WRN

WRN RecQ like helicase

Chromosome
8
Cytoband
8p12
Variants (rsID)
56

WRN is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 8 (region 8p12). Its official name is “WRN RecQ like helicase”. The reference table lists 56 variants (rsID) for this gene.

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Clinically classified variants

28 reference-table entries with clinical significance.

  • rs11574158Benignsingle nucleotide variantWerner syndrome
  • rs11574263Benignsingle nucleotide variantWerner syndrome
  • rs1346044Benignsingle nucleotide variantWerner syndrome
  • rs1800392Benignsingle nucleotide variantWerner syndrome
  • rs2230009Benignsingle nucleotide variantWerner syndrome
  • rs2230011Benignsingle nucleotide variantWerner syndrome
  • rs3087409Benignsingle nucleotide variantWerner syndrome
  • rs3087425Benignsingle nucleotide variantWerner syndrome
  • rs11574323Conflicting interpretationssingle nucleotide variantWerner syndrome
  • rs144116311Conflicting interpretationssingle nucleotide variantWerner syndrome
  • rs147802438Conflicting interpretationssingle nucleotide variantWerner syndrome
  • rs149565907Conflicting interpretationssingle nucleotide variantWerner syndrome
  • rs150148567Conflicting interpretationssingle nucleotide variantWerner syndrome
  • rs202148988Conflicting interpretationssingle nucleotide variantWerner syndrome
  • rs34477820Conflicting interpretationssingle nucleotide variantWerner syndrome
  • rs377226126Conflicting interpretationssingle nucleotide variantWerner syndrome
  • rs78488552Conflicting interpretationssingle nucleotide variantWerner syndrome
  • rs185468906Likely benignsingle nucleotide variantWerner syndrome
  • rs267607008Othersingle nucleotide variantWerner Syndrome
  • rs113993961Pathogenicsingle nucleotide variantWerner syndrome
  • rs17847577Pathogenicsingle nucleotide variantWerner syndrome|Medulloblastoma
  • rs281865160PathogenicDeletionWerner syndrome
  • rs142346721Uncertain significancesingle nucleotide variantWerner syndrome
  • rs144670883Uncertain significancesingle nucleotide variantWerner syndrome
  • rs202129203Uncertain significancesingle nucleotide variantWerner syndrome
  • rs61761625Uncertain significancesingle nucleotide variantWerner syndrome
  • rs281865158Not classifiedDuplicationWerner syndrome
  • rs281865159Not classifiedsingle nucleotide variantWerner 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.