Gene entry
SIM2
SIM bHLH transcription factor 2
- Chromosome
- 21
- Cytoband
- 21q22.13
- Variants (rsID)
- 21
SIM2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 21 (region 21q22.13). Its official name is “SIM bHLH transcription factor 2”. The reference table lists 21 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs2073601Not classifiedmissense_variantDown Syndrome|Chromosomal Triplication|Scoliosis
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.
