Gene entry
MLYCD
malonyl-CoA decarboxylase
- Chromosome
- 16
- Cytoband
- 16q23.3
- Variants (rsID)
- 15
MLYCD is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 16 (region 16q23.3). Its official name is “malonyl-CoA decarboxylase”. The reference table lists 15 variants (rsID) for this gene.
Clinically classified variants
4 reference-table entries with clinical significance.
- rs147617160Benignsingle nucleotide variantDeficiency of malonyl-CoA decarboxylase
- rs2278037Benignsingle nucleotide variantDeficiency of malonyl-CoA decarboxylase
- rs3815806Benignsingle nucleotide variantDeficiency of malonyl-CoA decarboxylase
- rs201973830Conflicting interpretationssingle nucleotide variantDeficiency of malonyl-CoA decarboxylase
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.