Gene entry
INF2
inverted formin 2
- Chromosome
- 14
- Cytoband
- 14q32.33
- Variants (rsID)
- 11
INF2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 14 (region 14q32.33). Its official name is “inverted formin 2”. The reference table lists 11 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs387907037Likely pathogenicsingle nucleotide variantCharcot-Marie-Tooth disease dominant intermediate E|Charcot-Marie-Tooth disease dominant intermediate E|Focal segmental glomerulosclerosis 5
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.