Gene entry
AXIN2
axin 2
- Chromosome
- 17
- Cytoband
- 17q24.1
- Variants (rsID)
- 37
AXIN2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 17 (region 17q24.1). Its official name is “axin 2”. The reference table lists 37 variants (rsID) for this gene.
Clinically classified variants
30 reference-table entries with clinical significance.
- rs138287857Benignsingle nucleotide variantOligodontia-cancer predisposition syndrome|Colorectal cancer|Aganglionic megacolon|Hereditary cancer-predisposing syndrome
- rs139871607Benignsingle nucleotide variantOligodontia-cancer predisposition syndrome|Oligodontia|Colorectal cancer|Hereditary cancer-predisposing syndrome
- rs143243661Benignsingle nucleotide variantOligodontia-cancer predisposition syndrome|Hereditary cancer-predisposing syndrome
- rs144099816Benignsingle nucleotide variantOligodontia-cancer predisposition syndrome|Hereditary cancer-predisposing syndrome
- rs200883019Benignsingle nucleotide variantOligodontia-cancer predisposition syndrome|Hereditary cancer-predisposing syndrome
- rs2240308Benignsingle nucleotide variantOligodontia-cancer predisposition syndrome|Hereditary cancer-predisposing syndrome
- rs7219582Benignsingle nucleotide variantOligodontia-cancer predisposition syndrome
- rs8081536Benignsingle nucleotide variantOligodontia-cancer predisposition syndrome|Hereditary cancer-predisposing syndrome
- rs9913621Benignsingle nucleotide variantHereditary cancer-predisposing syndrome|Oligodontia-cancer predisposition syndrome
- rs117688560Conflicting interpretationssingle nucleotide variantOligodontia-cancer predisposition syndrome|Hereditary cancer-predisposing syndrome|Malignant tumor of breast
- rs140344858Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Oligodontia-cancer predisposition syndrome
- rs143571197Conflicting interpretationssingle nucleotide variantOligodontia-cancer predisposition syndrome|Hereditary cancer-predisposing syndrome
- rs145007501Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Oligodontia-cancer predisposition syndrome|Oligodontia|Colorectal cancer|Colorectal cancer
- rs148691166Conflicting interpretationssingle nucleotide variantOligodontia-cancer predisposition syndrome|Hereditary cancer-predisposing syndrome
- rs148765149Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Oligodontia-cancer predisposition syndrome
- rs149764887Conflicting interpretationssingle nucleotide variantOligodontia-cancer predisposition syndrome|Hereditary cancer-predisposing syndrome|Colorectal cancer
- rs200201811Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Oligodontia-cancer predisposition syndrome
- rs200899695Conflicting interpretationssingle nucleotide variantOligodontia-cancer predisposition syndrome|Hereditary cancer-predisposing syndrome
- rs201531372Conflicting interpretationssingle nucleotide variantOligodontia-cancer predisposition syndrome|Hereditary cancer-predisposing syndrome
- rs376052287Conflicting interpretationssingle nucleotide variantOligodontia-cancer predisposition syndrome
- rs376584101Conflicting interpretationssingle nucleotide variantOligodontia-cancer predisposition syndrome|Hereditary cancer-predisposing syndrome
- rs529954883Conflicting interpretationssingle nucleotide variantOligodontia-cancer predisposition syndrome|Hereditary cancer-predisposing syndrome
- rs62640028Conflicting interpretationssingle nucleotide variantOligodontia-cancer predisposition syndrome|Hereditary cancer-predisposing syndrome
- rs745726935Conflicting interpretationsDuplicationOligodontia-cancer predisposition syndrome|Hereditary cancer-predisposing syndrome
- rs748143308Conflicting interpretationssingle nucleotide variantOligodontia-cancer predisposition syndrome|Hereditary cancer-predisposing syndrome
- rs761978806Conflicting interpretationssingle nucleotide variantOligodontia-cancer predisposition syndrome|Hereditary cancer-predisposing syndrome
- rs878854720Conflicting interpretationssingle nucleotide variantOligodontia-cancer predisposition syndrome
- rs886053272Conflicting interpretationssingle nucleotide variantOligodontia-cancer predisposition syndrome
- rs1060504488Likely benignsingle nucleotide variantOligodontia-cancer predisposition syndrome|Hereditary cancer-predisposing syndrome
- rs142670753Likely benignsingle nucleotide variantOligodontia-cancer predisposition syndrome|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.