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Gene

RPL17-C18orf32

RPL17-C18orf32 readthrough

Summary

Cytogenetic location
18q21.1
Locus type
readthrough

Curated reports relevant to this gene

No Genome Test report reads RPL17-C18orf32 yet. The test sequences your whole genome, so your data includes it all the same.

How a genome test reads RPL17-C18orf32

1

position in RPL17-C18orf32 where ClinVar classes a change as pathogenic or likely pathogenic

1 of them (100%) falls in a region short reads find hard.

  • Low mappability (1 site)Regions where 100 bp or 250 bp reads cannot be placed uniquely.

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

APA

Dante Labs. (n.d.). RPL17-C18orf32 gene: RPL17-C18orf32 readthrough. Retrieved 17 October 2026, from https://dantelabs.com/genes/rpl17-c18orf32

Vancouver

Dante Labs. RPL17-C18orf32 gene: RPL17-C18orf32 readthrough [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/rpl17-c18orf32

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