Gene entry
MCM8
minichromosome maintenance 8 homologous recombination repair factor
- Chromosome
- 20
- Cytoband
- 20p12.3
- Variants (rsID)
- 21
MCM8 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 20 (region 20p12.3). Its official name is “minichromosome maintenance 8 homologous recombination repair factor”. The reference table lists 21 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs236110Not classifiedmissense_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.
