Gene
ST20-MTHFS
ST20-MTHFS readthrough
- HGNC 44655(opens in a new tab)
- Ensembl gene ENSG00000259332(opens in a new tab)
- NCBI Gene 100528021(opens in a new tab)
Summary
- Cytogenetic location
- 15q25.1
- Locus type
- readthrough
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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No Genome Test report reads ST20-MTHFS yet. The test sequences your whole genome, so your data includes it all the same.
How a genome test reads ST20-MTHFS
1
position in ST20-MTHFS 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.). ST20-MTHFS gene: ST20-MTHFS readthrough. Retrieved 17 October 2026, from https://dantelabs.com/genes/st20-mthfs
Dante Labs. ST20-MTHFS gene: ST20-MTHFS readthrough [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/st20-mthfs
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