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.
