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Gene entry

ADGRG1

adhesion G protein-coupled receptor G1

Chromosome
16
Cytoband
16q21
Variants (rsID)
45

ADGRG1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 16 (region 16q21). Its official name is “adhesion G protein-coupled receptor G1”. The reference table lists 45 variants (rsID) for this gene.

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Clinically classified variants

15 reference-table entries with clinical significance.

  • rs17379472Benignsingle nucleotide variantBilateral frontoparietal polymicrogyria
  • rs1801255Benignsingle nucleotide variantBilateral frontoparietal polymicrogyria
  • rs186479054Benignsingle nucleotide variantBilateral frontoparietal polymicrogyria
  • rs74326170Benignsingle nucleotide variantBilateral frontoparietal polymicrogyria
  • rs111939130Conflicting interpretationssingle nucleotide variantBilateral frontoparietal polymicrogyria
  • rs112775979Conflicting interpretationssingle nucleotide variantBilateral frontoparietal polymicrogyria
  • rs113358058Conflicting interpretationssingle nucleotide variantBilateral frontoparietal polymicrogyria
  • rs147495708Conflicting interpretationssingle nucleotide variantBilateral frontoparietal polymicrogyria
  • rs121908462Likely pathogenicsingle nucleotide variantBilateral frontoparietal polymicrogyria|Abnormality of the nervous system
  • rs587776623Likely pathogenicsingle nucleotide variantBilateral frontoparietal polymicrogyria
  • rs121908464Pathogenicsingle nucleotide variantBilateral frontoparietal polymicrogyria
  • rs121908465Pathogenicsingle nucleotide variantBilateral frontoparietal polymicrogyria
  • rs121908466Pathogenicsingle nucleotide variantBilateral frontoparietal polymicrogyria
  • rs146278035Pathogenicsingle nucleotide variantBilateral frontoparietal polymicrogyria|Inborn genetic diseases
  • rs797045602PathogenicDuplicationBilateral frontoparietal polymicrogyria

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.