Gene entry
INS-IGF2
INS-IGF2 readthrough
- Chromosome
- 11
- Cytoband
- 11p15.5
- Variants (rsID)
- 6
INS-IGF2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 11 (region 11p15.5). Its official name is “INS-IGF2 readthrough”. The reference table lists 6 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs10770125Not classifiedmissense_variantGestational Diabetes|Microvascular Complications of Diabetes 6|Microvascular Complications of Diabetes 4|Microvascular Complications of Diabetes 3|Microvascular Complications of Diabetes 7
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.