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Gene entry

ITGA7

integrin subunit alpha 7

Chromosome
12
Cytoband
12q13.2
Variants (rsID)
29

ITGA7 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 12 (region 12q13.2). Its official name is “integrin subunit alpha 7”. The reference table lists 29 variants (rsID) for this gene.

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Clinically classified variants

23 reference-table entries with clinical significance.

  • rs140030984Benignsingle nucleotide variantCongenital muscular dystrophy due to integrin alpha-7 deficiency
  • rs148170949Benignsingle nucleotide variantCongenital muscular dystrophy due to integrin alpha-7 deficiency
  • rs148190047Benignsingle nucleotide variantCongenital muscular dystrophy due to integrin alpha-7 deficiency
  • rs17117879Benignsingle nucleotide variantCongenital muscular dystrophy due to integrin alpha-7 deficiency
  • rs17117883Benignsingle nucleotide variantCongenital muscular dystrophy due to integrin alpha-7 deficiency
  • rs17854601Benignsingle nucleotide variantCongenital muscular dystrophy due to integrin alpha-7 deficiency
  • rs1800974Benignsingle nucleotide variantCongenital muscular dystrophy due to integrin alpha-7 deficiency
  • rs370741662Benignsingle nucleotide variantCongenital muscular dystrophy due to integrin alpha-7 deficiency
  • rs61733050Benignsingle nucleotide variantCongenital muscular dystrophy due to integrin alpha-7 deficiency
  • rs61733963Benignsingle nucleotide variantCongenital muscular dystrophy due to integrin alpha-7 deficiency
  • rs74867235Benignsingle nucleotide variantCongenital muscular dystrophy due to integrin alpha-7 deficiency
  • rs7971022Benignsingle nucleotide variantCongenital muscular dystrophy due to integrin alpha-7 deficiency
  • rs79745402Benignsingle nucleotide variantCongenital muscular dystrophy due to integrin alpha-7 deficiency
  • rs144983062Conflicting interpretationssingle nucleotide variantCongenital muscular dystrophy due to integrin alpha-7 deficiency
  • rs145463677Conflicting interpretationssingle nucleotide variantCongenital muscular dystrophy due to integrin alpha-7 deficiency
  • rs148641361Conflicting interpretationssingle nucleotide variantCongenital muscular dystrophy due to integrin alpha-7 deficiency
  • rs149028067Conflicting interpretationssingle nucleotide variantCongenital muscular dystrophy due to integrin alpha-7 deficiency
  • rs149081471Conflicting interpretationssingle nucleotide variantCongenital muscular dystrophy due to integrin alpha-7 deficiency
  • rs149963176Conflicting interpretationssingle nucleotide variantCongenital muscular dystrophy due to integrin alpha-7 deficiency
  • rs181711509Conflicting interpretationssingle nucleotide variantCongenital muscular dystrophy due to integrin alpha-7 deficiency
  • rs77929806Likely benignsingle nucleotide variantCongenital muscular dystrophy due to integrin alpha-7 deficiency
  • rs143749139Uncertain significancesingle nucleotide variantCongenital muscular dystrophy due to integrin alpha-7 deficiency
  • rs76938320Uncertain significancesingle nucleotide variantCongenital muscular dystrophy due to integrin alpha-7 deficiency

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.