Gene entry
DMGDH
dimethylglycine dehydrogenase
- Chromosome
- 5
- Cytoband
- 5q14.1
- Variants (rsID)
- 29
DMGDH is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 5 (region 5q14.1). Its official name is “dimethylglycine dehydrogenase”. The reference table lists 29 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs77116243Benignsingle nucleotide variant
- rs41272262Likely benignsingle nucleotide variant
- rs121908331Likely pathogenicsingle nucleotide variantDimethylglycine dehydrogenase deficiency
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.