Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Gene entry

PCDH15

protocadherin related 15

Chromosome
10
Cytoband
10q21.1
Variants (rsID)
409

PCDH15 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 10 (region 10q21.1). Its official name is “protocadherin related 15”. The reference table lists 409 variants (rsID) for this gene.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Clinically classified variants

45 reference-table entries with clinical significance.

  • rs111033362Benignsingle nucleotide variantUsher syndrome type 1|Usher syndrome type 1F
  • rs111033496Benignsingle nucleotide variantUsher syndrome type 1|Usher syndrome type 1F
  • rs113363047BenignMicrosatelliteUsher syndrome type 1|Usher syndrome type 1F|USHER SYNDROME, TYPE ID/F, DIGENIC
  • rs147835286Benignsingle nucleotide variantUsher syndrome type 1
  • rs148533341Benignsingle nucleotide variant
  • rs148718874Benignsingle nucleotide variantUsher syndrome type 1|Usher syndrome type 1F|Autosomal recessive nonsyndromic hearing loss 23
  • rs149478475Benignsingle nucleotide variantUsher syndrome type 1|Usher syndrome type 1F
  • rs149867749Benignsingle nucleotide variantUsher syndrome type 1
  • rs2135720Benignsingle nucleotide variantUsher syndrome type 1|Usher syndrome type 1F
  • rs34164469Benignsingle nucleotide variantUsher syndrome type 1|Usher syndrome type 1F|Autosomal recessive nonsyndromic hearing loss 23
  • rs41274622Benignsingle nucleotide variant
  • rs41274634Benignsingle nucleotide variantUsher syndrome type 1|Usher syndrome type 1F
  • rs41304641Benignsingle nucleotide variantUsher syndrome type 1|Usher syndrome type 1F
  • rs41307518Benignsingle nucleotide variantUsher syndrome type 1|Usher syndrome type 1F
  • rs4935502Benignsingle nucleotide variantUsher syndrome type 1|Usher syndrome type 1F
  • rs61730754Benignsingle nucleotide variantUsher syndrome type 1
  • rs61731363Benignsingle nucleotide variantUsher syndrome type 1F|Usher syndrome type 1
  • rs61731389Benignsingle nucleotide variantUsher syndrome type 1|Usher syndrome type 1F|Autosomal recessive nonsyndromic hearing loss 23
  • rs61735473Benignsingle nucleotide variantUsher syndrome type 1|Usher syndrome type 1F
  • rs61862390Benignsingle nucleotide variantUsher syndrome type 1F|Usher syndrome type 1
  • rs74609306Benignsingle nucleotide variant
  • rs7921598Benignsingle nucleotide variantUsher syndrome type 1|Usher syndrome type 1F
  • rs111033445Conflicting interpretationssingle nucleotide variantUsher syndrome type 1|Usher syndrome type 1F
  • rs111033499Conflicting interpretationssingle nucleotide variantUsher syndrome type 1|Usher syndrome type 1F
  • rs111033516Conflicting interpretationssingle nucleotide variantUsher syndrome type 1|Usher syndrome type 1F
  • rs138010738Conflicting interpretationssingle nucleotide variantUsher syndrome type 1|Usher syndrome type 1F
  • rs139668636Conflicting interpretationssingle nucleotide variantUsher syndrome type 1
  • rs143058902Conflicting interpretationssingle nucleotide variant
  • rs143827620Conflicting interpretationssingle nucleotide variantUsher syndrome type 1
  • rs144261647Conflicting interpretationssingle nucleotide variantUsher syndrome type 1|Usher syndrome type 1F
  • rs145017164Conflicting interpretationssingle nucleotide variantUsher syndrome type 1D|Usher syndrome type 1F|Autosomal recessive nonsyndromic hearing loss 23|Usher syndrome type 1|Usher syndrome type 1F
  • rs151119732Conflicting interpretationssingle nucleotide variantUsher syndrome type 1|Usher syndrome type 1F
  • rs184144118Conflicting interpretationssingle nucleotide variantUsher syndrome type 1|Usher syndrome type 1F
  • rs191577774Conflicting interpretationssingle nucleotide variantUsher syndrome type 1
  • rs201816080Conflicting interpretationssingle nucleotide variantUsher syndrome type 1|Usher syndrome type 1F
  • rs375134176Conflicting interpretationssingle nucleotide variantUsher syndrome type 1|Usher syndrome type 1F
  • rs397517461Conflicting interpretationssingle nucleotide variantUsher syndrome type 1|Usher syndrome type 1F
  • rs61735479Conflicting interpretationssingle nucleotide variantUsher syndrome type 1|Usher syndrome type 1F
  • rs137853003Likely pathogenicsingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 23|Rare genetic deafness
  • rs111033260Pathogenicsingle nucleotide variantUsher syndrome type 1F|Usher syndrome type 1G|Usher syndrome type 1|Autosomal recessive nonsyndromic hearing loss 23|Usher syndrome type 1D|Usher syndrome type 1F|Rare genetic deafness|Autosomal recessive nonsyndromic hearing loss 23|Usher syndrome type 1D
  • rs137853001Pathogenicsingle nucleotide variantUsher syndrome type 1F|Autosomal recessive nonsyndromic hearing loss 23|Rare genetic deafness
  • rs202033121Pathogenicsingle nucleotide variantUsher syndrome type 1F|Autosomal recessive nonsyndromic hearing loss 23|Usher syndrome type 1D|Usher syndrome type 1F|Rare genetic deafness
  • rs139175351Uncertain significancesingle nucleotide variantUsher syndrome type 1F|Usher syndrome type 1D
  • rs142512524Uncertain significancesingle nucleotide variantUsher syndrome type 1|Usher syndrome type 1D|Usher syndrome type 1F|Autosomal recessive nonsyndromic hearing loss 23|Hearing impairment|Autosomal recessive nonsyndromic hearing loss 23|Usher syndrome type 1F
  • rs145037203Uncertain significancesingle nucleotide variantUsher syndrome type 1F

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.