Gene
INS-IGF2
INS-IGF2 readthrough
- HGNC 33527(opens in a new tab)
- Ensembl gene ENSG00000129965(opens in a new tab)
- NCBI Gene 723961(opens in a new tab)
Summary
- Cytogenetic location
- 11p15.5
- Locus type
- readthrough
- Very high
- Confident
- Low
- Very low
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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No Genome Test report reads INS-IGF2 yet. The test sequences your whole genome, so your data includes it all the same.
How a genome test reads INS-IGF2
1
position in INS-IGF2 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.). INS-IGF2 gene: INS-IGF2 readthrough. Retrieved 16 October 2026, from https://dantelabs.com/genes/ins-igf2
Dante Labs. INS-IGF2 gene: INS-IGF2 readthrough [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/ins-igf2
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