Gene entry
MCM9
minichromosome maintenance 9 homologous recombination repair factor
- Chromosome
- 6
- Cytoband
- 6q22.31
- Variants (rsID)
- 15
MCM9 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 6 (region 6q22.31). Its official name is “minichromosome maintenance 9 homologous recombination repair factor”. The reference table lists 15 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs78231991Likely benignsingle nucleotide variantPremature ovarian insufficiency|Premature ovarian failure
- rs79670608Not 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.