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Gene entry

WDR62

WD repeat domain 62

Chromosome
19
Cytoband
19q13.12
Variants (rsID)
30

WDR62 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 19 (region 19q13.12). Its official name is “WD repeat domain 62”. The reference table lists 30 variants (rsID) for this gene.

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Clinically classified variants

26 reference-table entries with clinical significance.

  • rs1008328Benignsingle nucleotide variantMicrocephaly 2, primary, autosomal recessive, with or without cortical malformations
  • rs111294536Benignsingle nucleotide variantMicrocephaly 2, primary, autosomal recessive, with or without cortical malformations
  • rs12327568Benignsingle nucleotide variantMicrocephaly 2, primary, autosomal recessive, with or without cortical malformations
  • rs143309981Benignsingle nucleotide variantMicrocephaly 2, primary, autosomal recessive, with or without cortical malformations
  • rs148415080Benignsingle nucleotide variantMicrocephaly 2, primary, autosomal recessive, with or without cortical malformations
  • rs182467995Benignsingle nucleotide variantMicrocephaly 2, primary, autosomal recessive, with or without cortical malformations
  • rs187029707Benignsingle nucleotide variantMicrocephaly 2, primary, autosomal recessive, with or without cortical malformations
  • rs2285745Benignsingle nucleotide variantMicrocephaly 2, primary, autosomal recessive, with or without cortical malformations
  • rs2301734Benignsingle nucleotide variantMicrocephaly 2, primary, autosomal recessive, with or without cortical malformations
  • rs35811023Benignsingle nucleotide variantMicrocephaly 2, primary, autosomal recessive, with or without cortical malformations
  • rs61741470Benignsingle nucleotide variantMicrocephaly 2, primary, autosomal recessive, with or without cortical malformations
  • rs61743589Benignsingle nucleotide variantMicrocephaly 2, primary, autosomal recessive, with or without cortical malformations
  • rs61744321Benignsingle nucleotide variantMicrocephaly 2, primary, autosomal recessive, with or without cortical malformations
  • rs117887683Conflicting interpretationssingle nucleotide variantMicrocephaly 2, primary, autosomal recessive, with or without cortical malformations
  • rs139749569Conflicting interpretationssingle nucleotide variantMicrocephaly 2, primary, autosomal recessive, with or without cortical malformations
  • rs144697999Conflicting interpretationssingle nucleotide variantMicrocephaly 2, primary, autosomal recessive, with or without cortical malformations
  • rs146274964Conflicting interpretationssingle nucleotide variantMicrocephaly 2, primary, autosomal recessive, with or without cortical malformations
  • rs146485488Conflicting interpretationssingle nucleotide variant
  • rs147652186Conflicting interpretationssingle nucleotide variantMicrocephaly 2, primary, autosomal recessive, with or without cortical malformations
  • rs147875659Conflicting interpretationssingle nucleotide variantMicrocephaly 2, primary, autosomal recessive, with or without cortical malformations|Autosomal recessive primary microcephaly
  • rs202109439Conflicting interpretationssingle nucleotide variantMicrocephaly 2, primary, autosomal recessive, with or without cortical malformations|Intellectual disability
  • rs757294519Conflicting interpretationssingle nucleotide variantMicrocephaly 2, primary, autosomal recessive, with or without cortical malformations
  • rs765001215Conflicting interpretationssingle nucleotide variantMicrocephaly 2, primary, autosomal recessive, with or without cortical malformations
  • rs376633424Pathogenicsingle nucleotide variant
  • rs199673795Uncertain significancesingle nucleotide variant
  • rs377731205Uncertain significancesingle nucleotide variantMicrocephaly 2, primary, autosomal recessive, with or without cortical malformations

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.