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Gene entry

HNRNPDL

heterogeneous nuclear ribonucleoprotein D like

Chromosome
4
Cytoband
4q21.22
Variants (rsID)
5

HNRNPDL is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 4 (region 4q21.22). Its official name is “heterogeneous nuclear ribonucleoprotein D like”. The reference table lists 5 variants (rsID) for this gene.

Clinically classified variants

2 reference-table entries with clinical significance.

  • rs200595389Likely benignsingle nucleotide variantAutosomal dominant limb-girdle muscular dystrophy type 1G
  • rs201774571Likely benignsingle nucleotide variantAutosomal dominant limb-girdle muscular dystrophy type 1G

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.