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Gene entry

WHRN

whirlin

Chromosome
9
Cytoband
9q32
Variants (rsID)
47

WHRN is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 9 (region 9q32). Its official name is “whirlin”. The reference table lists 47 variants (rsID) for this gene.

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Clinically classified variants

20 reference-table entries with clinical significance.

  • rs117352600Benignsingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 31|Usher syndrome type 2D
  • rs117592152Benignsingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 31|Usher syndrome type 2D
  • rs2274160Benignsingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 31|Usher syndrome type 2D
  • rs2296262Benignsingle nucleotide variant
  • rs34252199Benignsingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 31|Usher syndrome type 2D
  • rs111033459Conflicting interpretationssingle nucleotide variantUsher syndrome type 2D|Autosomal recessive nonsyndromic hearing loss 31
  • rs139337135Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 31|Usher syndrome type 2D
  • rs142990800Conflicting interpretationssingle nucleotide variant
  • rs143443833Conflicting interpretationssingle nucleotide variantUsher syndrome type 2D|Autosomal recessive nonsyndromic hearing loss 31
  • rs146273185Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 31|Usher syndrome type 2D
  • rs146655362Conflicting interpretationssingle nucleotide variantUsher syndrome type 2D|Autosomal recessive nonsyndromic hearing loss 31|Autosomal recessive nonsyndromic hearing loss 31|Usher syndrome type 2D
  • rs373552185Conflicting interpretationssingle nucleotide variant
  • rs45527543Conflicting interpretationssingle nucleotide variantRetinitis pigmentosa-deafness syndrome|Autosomal recessive nonsyndromic hearing loss 31|Usher syndrome type 2D
  • rs535492772Conflicting interpretationssingle nucleotide variant
  • rs55966714Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 31|Usher syndrome type 2D
  • rs56059137Conflicting interpretationssingle nucleotide variantUsher syndrome type 2D|Autosomal recessive nonsyndromic hearing loss 31
  • rs61743618Conflicting interpretationssingle nucleotide variantUsher syndrome type 2D|Autosomal recessive nonsyndromic hearing loss 31
  • rs79572315Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 31|Usher syndrome type 2D
  • rs149897775Uncertain significancesingle nucleotide variant
  • rs55749855Uncertain 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.