Gene entry
PARN
poly(A)-specific ribonuclease
- Chromosome
- 16
- Cytoband
- 16p13.12
- Variants (rsID)
- 26
PARN is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 16 (region 16p13.12). Its official name is “poly(A)-specific ribonuclease”. The reference table lists 26 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs138984302Benignsingle nucleotide variantDyskeratosis congenita, autosomal recessive 6|Pulmonary fibrosis and/or bone marrow failure, Telomere-related, 4
- rs201765587Conflicting interpretationssingle nucleotide variantDyskeratosis congenita, autosomal recessive 6|Pulmonary fibrosis and/or bone marrow failure, Telomere-related, 4|Dyskeratosis congenita, autosomal recessive 6
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.