Gene entry
MGME1
mitochondrial genome maintenance exonuclease 1
- Chromosome
- 20
- Cytoband
- 20p11.23
- Variants (rsID)
- 7
MGME1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 20 (region 20p11.23). Its official name is “mitochondrial genome maintenance exonuclease 1”. The reference table lists 7 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs143811282Benignsingle nucleotide variant
- rs143417446Conflicting interpretationssingle nucleotide variantMitochondrial DNA depletion syndrome 11
- rs76599088Conflicting interpretationssingle nucleotide variantMitochondrial DNA depletion syndrome 11
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.