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Gene entry

GLIS3

GLIS family zinc finger 3

Chromosome
9
Cytoband
9p24.2
Variants (rsID)
173

GLIS3 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 9 (region 9p24.2). Its official name is “GLIS family zinc finger 3”. The reference table lists 173 variants (rsID) for this gene.

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Clinically classified variants

9 reference-table entries with clinical significance.

  • rs117876027Benignsingle nucleotide variantNeonatal diabetes mellitus with congenital hypothyroidism
  • rs146131512Benignsingle nucleotide variantMonogenic diabetes|Neonatal diabetes mellitus with congenital hypothyroidism
  • rs148199056Benignsingle nucleotide variantNeonatal diabetes mellitus with congenital hypothyroidism|Monogenic diabetes|Diabetes mellitus
  • rs76094493Benignsingle nucleotide variantNeonatal diabetes mellitus with congenital hypothyroidism|Monogenic diabetes
  • rs138497710Conflicting interpretationssingle nucleotide variantMonogenic diabetes|Neonatal diabetes mellitus with congenital hypothyroidism
  • rs141467694Conflicting interpretationssingle nucleotide variantNeonatal diabetes mellitus with congenital hypothyroidism
  • rs148572278Conflicting interpretationssingle nucleotide variantNeonatal diabetes mellitus with congenital hypothyroidism|Monogenic diabetes
  • rs150310830Likely benignsingle nucleotide variantCongenital aniridia
  • rs2281731Not classifiedintron_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.