Gene entry
KMT2A
lysine methyltransferase 2A
- Chromosome
- 11
- Cytoband
- 11q23.3
- Variants (rsID)
- 18
KMT2A is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 11 (region 11q23.3). Its official name is “lysine methyltransferase 2A”. The reference table lists 18 variants (rsID) for this gene.
Clinically classified variants
5 reference-table entries with clinical significance.
- rs150804738Benignsingle nucleotide variant
- rs9332772Benignsingle nucleotide variant
- rs150328852Conflicting interpretationssingle nucleotide variant
- rs1057520053Pathogenicsingle nucleotide variant
- rs886041856Pathogenicsingle nucleotide variantintellectual deficiency|Wiedemann-Steiner syndrome|Inborn genetic diseases
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.