Gene entry
RNASEH2B
ribonuclease H2 subunit B
- Chromosome
- 13
- Cytoband
- 13q14.3
- Variants (rsID)
- 12
RNASEH2B is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 13 (region 13q14.3). Its official name is “ribonuclease H2 subunit B”. The reference table lists 12 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs75184679Pathogenicsingle nucleotide variantAicardi-Goutieres syndrome 2|Aicardi Goutieres syndrome|Cerebral palsy|Abnormality of the nervous system
- rs150363383Uncertain significancesingle nucleotide variantAicardi-Goutieres syndrome 2
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.