Gene entry
AIP
AHR interacting HSP90 co-chaperone
- Chromosome
- 11
- Cytoband
- 11q13.2
- Variants (rsID)
- 7
AIP is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 11 (region 11q13.2). Its official name is “AHR interacting HSP90 co-chaperone”. The reference table lists 7 variants (rsID) for this gene.
Clinically classified variants
5 reference-table entries with clinical significance.
- rs104894190Conflicting interpretationssingle nucleotide variantPituitary dependent hypercortisolism|Somatotroph adenoma|Hereditary cancer-predisposing syndrome|Dopamine agonists response
- rs1063385Conflicting interpretationssingle nucleotide variantSomatotroph adenoma|Hereditary cancer-predisposing syndrome
- rs116940576Conflicting interpretationssingle nucleotide variantSomatotroph adenoma|Hereditary cancer-predisposing syndrome
- rs145047094Conflicting interpretationssingle nucleotide variantSomatotroph adenoma|Hereditary cancer-predisposing syndrome|Familial isolated pituitary adenoma
- rs147931650Conflicting interpretationssingle nucleotide variantSomatotroph adenoma|Hereditary cancer-predisposing syndrome
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.