Gene entry
EPHA2
EPH receptor A2
- Chromosome
- 1
- Cytoband
- 1p36.13
- Variants (rsID)
- 23
EPHA2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1p36.13). Its official name is “EPH receptor A2”. The reference table lists 23 variants (rsID) for this gene.
Clinically classified variants
9 reference-table entries with clinical significance.
- rs112285834Benignsingle nucleotide variantCataract 6 multiple types
- rs2291804Benignsingle nucleotide variantCataract 6 multiple types
- rs34192549Benignsingle nucleotide variantSquamous cell lung carcinoma|Cataract 6 multiple types
- rs35903225Benignsingle nucleotide variantCataract 6 multiple types
- rs3754334Benignsingle nucleotide variantCataract 6 multiple types
- rs55747232Benignsingle nucleotide variantCataract 6 multiple types
- rs116506614Conflicting interpretationssingle nucleotide variantCataract 6, age-related cortical|Cataract 6 multiple types|Cortical senile cataract
- rs145592908Conflicting interpretationssingle nucleotide variantCataract 6 multiple types
- rs139176878Likely benignsingle nucleotide variantCataract 6 multiple types
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.