Gene
SNORD9
small nucleolar RNA, C/D box 9
- HGNC 32705↗(opens in a new tab)
- Ensembl gene ENSG00000199436↗(opens in a new tab)
- NCBI Gene 692053↗(opens in a new tab)
Summary
- Cytogenetic location
- 14q11.2
- Also known as
- mgU6-53B
- Locus type
- RNA, small nucleolar
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
Read SNORD9, and the rest of your genome, with one test.
From $449Free shipping · Results in 6–8 weeks
Get my Genome TestCurated reports relevant to this gene
No Genome Test report reads SNORD9 yet. The test sequences your whole genome, so your data includes it all the same.
How a genome test reads SNORD9
1
position in SNORD9 where ClinVar classes a change as pathogenic or likely pathogenic
None of them falls in a region short reads find hard.
External links
Where this comes from
- HGNC: the gene's symbol, name, other symbols and location.
- ClinVar and the GIAB stratifications: known disease-causing sites, and the regions short reads find hard.
- Data release 2026.10.16-c6eea6bf.
Cite this page
Dante Labs. (n.d.). SNORD9 gene: small nucleolar RNA, C/D box 9. Retrieved 17 October 2026, from https://dantelabs.com/genes/snord9
Dante Labs. SNORD9 gene: small nucleolar RNA, C/D box 9 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/snord9
One test. A lifetime of answers.
From $449Free shipping · Results in 6–8 weeks