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Gene entry

HNRNPA1

heterogeneous nuclear ribonucleoprotein A1

Chromosome
12
Cytoband
12q13.13
Variants (rsID)
21

HNRNPA1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 12 (region 12q13.13). Its official name is “heterogeneous nuclear ribonucleoprotein A1”. The reference table lists 21 variants (rsID) for this gene.

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Clinically classified variants

20 reference-table entries with clinical significance.

  • rs3206707Likely benignsingle nucleotide variantRelapsing remitting multiple sclerosis
  • rs483353026Likely benignsingle nucleotide variantRelapsing remitting multiple sclerosis
  • rs483353027Likely benignsingle nucleotide variantRelapsing remitting multiple sclerosis
  • rs483353040Likely benignsingle nucleotide variantChronic progressive multiple sclerosis
  • rs483353041Likely benignsingle nucleotide variantChronic progressive multiple sclerosis
  • rs483353042Likely benignsingle nucleotide variantChronic progressive multiple sclerosis
  • rs483353043Likely benignsingle nucleotide variantChronic progressive multiple sclerosis
  • rs483353022Likely pathogenicsingle nucleotide variantChronic progressive multiple sclerosis
  • rs483353024Likely pathogenicsingle nucleotide variantRelapsing remitting multiple sclerosis
  • rs483353029Likely pathogenicsingle nucleotide variantChronic progressive multiple sclerosis
  • rs483353030Likely pathogenicsingle nucleotide variantChronic progressive multiple sclerosis
  • rs483353034Likely pathogenicsingle nucleotide variantChronic progressive multiple sclerosis
  • rs483353035Likely pathogenicsingle nucleotide variantChronic progressive multiple sclerosis
  • rs483353036Likely pathogenicsingle nucleotide variantChronic progressive multiple sclerosis
  • rs483353038Likely pathogenicsingle nucleotide variantChronic progressive multiple sclerosis
  • rs483353039Likely pathogenicsingle nucleotide variantChronic progressive multiple sclerosis
  • rs483353031Pathogenicsingle nucleotide variantChronic progressive multiple sclerosis
  • rs483353020Uncertain significancesingle nucleotide variantRelapsing remitting multiple sclerosis
  • rs483353021Uncertain significancesingle nucleotide variantRelapsing remitting multiple sclerosis
  • rs483353037Uncertain significancesingle nucleotide variantChronic progressive multiple sclerosis

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.