Gene entry
SOBP
sine oculis binding protein homolog
- Chromosome
- 6
- Cytoband
- 6q21
- Variants (rsID)
- 37
SOBP is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 6 (region 6q21). Its official name is “sine oculis binding protein homolog”. The reference table lists 37 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs148915050Benignsingle nucleotide variant
- rs200006380Uncertain significancesingle nucleotide variant
- rs201319446Uncertain significancesingle nucleotide variantIntellectual disability, anterior maxillary protrusion, and strabismus
Other listed variants
- rs846983
- rs1321551
- rs1527874
- rs2818258
- rs2818259
- rs3778579
- rs3800209
- rs4440495
- rs6915710
- rs6924588
- rs6936145
- rs6940398
- rs7751374
- rs9373952
- rs9386647
- rs12197661
- rs12204977
- rs17068251
- rs57552845
- rs61526852
- rs62428431
- rs72945662
- rs73518913
- rs77948734
- rs78032258
- rs80041093
- rs112249318
- rs116869455
- rs116878897
- rs117291189
- rs117530454
- rs118029213
- rs118188175
- rs139988156
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.