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Gene entry

GLI2

GLI family zinc finger 2

Chromosome
2
Cytoband
2q14.2
Variants (rsID)
71

GLI2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 2 (region 2q14.2). Its official name is “GLI family zinc finger 2”. The reference table lists 71 variants (rsID) for this gene.

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Clinically classified variants

6 reference-table entries with clinical significance.

  • rs114376238Benignsingle nucleotide variantHoloprosencephaly 9|Holoprosencephaly 9|Postaxial polydactyly-anterior pituitary anomalies-facial dysmorphism syndrome
  • rs114814747Benignsingle nucleotide variantHoloprosencephaly 9|Holoprosencephaly 9|Postaxial polydactyly-anterior pituitary anomalies-facial dysmorphism syndrome
  • rs13008360Benignsingle nucleotide variantHoloprosencephaly 9|Postaxial polydactyly-anterior pituitary anomalies-facial dysmorphism syndrome|Holoprosencephaly 9
  • rs144372453Benignsingle nucleotide variantHoloprosencephaly 9|Holoprosencephaly 9|Postaxial polydactyly-anterior pituitary anomalies-facial dysmorphism syndrome
  • rs146207623Benignsingle nucleotide variantHoloprosencephaly 9|Postaxial polydactyly-anterior pituitary anomalies-facial dysmorphism syndrome|Holoprosencephaly 9
  • rs149091975Conflicting interpretationssingle nucleotide variantHoloprosencephaly 1|Holoprosencephaly 9|Postaxial polydactyly-anterior pituitary anomalies-facial dysmorphism syndrome|Holoprosencephaly 9

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.