Gene
MIR6886
microRNA 6886
- HGNC 50121↗(opens in a new tab)
- Ensembl gene ENSG00000284553↗(opens in a new tab)
- NCBI Gene 102465534↗(opens in a new tab)
Summary
- Cytogenetic location
- 19p13.2
- Also known as
- hsa-mir-6886
- Locus type
- MicroRNA (miRNA)
This page as data
Add .json to the page's address, or ask for application/json, to read it as JSON.
library(jsonlite)
url <- "https://dantelabs.com/genes/mir6886.json"
page <- fromJSON(url)
page$gene$nameRead MIR6886, and the rest of your genome, with one test.
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No Genome Test report reads MIR6886 yet. The test sequences your whole genome, so your data includes it all the same.
Sequencing MIR6886
3
positions in MIR6886 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 2026.10.17-8666dff2.
Cite this page
Dante Labs. (n.d.). MIR6886 gene: microRNA 6886. Retrieved 17 October 2026, from https://dantelabs.com/genes/mir6886
Dante Labs. MIR6886 gene: microRNA 6886 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/mir6886
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