Gene entry
RAI1
retinoic acid induced 1
- Chromosome
- 17
- Cytoband
- 17p11.2
- Variants (rsID)
- 37
RAI1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 17 (region 17p11.2). Its official name is “retinoic acid induced 1”. The reference table lists 37 variants (rsID) for this gene.
Clinically classified variants
11 reference-table entries with clinical significance.
- rs113208290Benignsingle nucleotide variantHistory of neurodevelopmental disorder
- rs11649804Benignsingle nucleotide variantSmith-Magenis syndrome|History of neurodevelopmental disorder
- rs151290050Benignsingle nucleotide variantHistory of neurodevelopmental disorder
- rs142981643Conflicting interpretationssingle nucleotide variantHistory of neurodevelopmental disorder
- rs147481626Conflicting interpretationssingle nucleotide variantHistory of neurodevelopmental disorder
- rs200719553Conflicting interpretationssingle nucleotide variantHistory of neurodevelopmental disorder|Smith-Magenis syndrome
- rs201393598Conflicting interpretationssingle nucleotide variantHistory of neurodevelopmental disorder
- rs202158738Conflicting interpretationssingle nucleotide variantHistory of neurodevelopmental disorder
- rs368106957Conflicting interpretationssingle nucleotide variant
- rs755572135Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 9|Smith-Magenis syndrome
- rs376044849Pathogenicsingle nucleotide variant
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.