Gene entry
KMT2C
lysine methyltransferase 2C
- Chromosome
- 7
- Cytoband
- 7q36.1
- Variants (rsID)
- 52
KMT2C is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 7 (region 7q36.1). Its official name is “lysine methyltransferase 2C”. The reference table lists 52 variants (rsID) for this gene.
Clinically classified variants
10 reference-table entries with clinical significance.
- rs13231116Benignsingle nucleotide variant
- rs140432708Benignsingle nucleotide variant
- rs142835638Benignsingle nucleotide variant
- rs148585727Benignsingle nucleotide variant
- rs74483926Benignsingle nucleotide variant
- rs77652527Benignsingle nucleotide variant
- rs138845109Conflicting interpretationssingle nucleotide variantatypical cerebral palsy
- rs140719911Likely benignsingle nucleotide variant
- rs140919432Likely benignsingle nucleotide variant
- rs200302468Not classifiedsingle nucleotide variant
Other listed variants
- rs3800836
- rs6464211
- rs6966258
- rs7787666
- rs9969322
- rs10252263
- rs11763960
- rs12703197
- rs13230351
- rs28480344
- rs34964784
- rs61730540
- rs71541758
- rs73164557
- rs75797448
- rs76520526
- rs78717543
- rs79669552
- rs80168150
- rs113978215
- rs116089370
- rs117169209
- rs117443780
- rs138111015
- rs139572807
- rs140332170
- rs140834550
- rs141106704
- rs145733369
- rs145953124
- rs146424878
- rs146952256
- rs147416712
- rs148065717
- rs148549720
- rs149653107
- rs187401695
- rs199588302
- rs199592124
- rs200173988
- rs200919055
- rs201164931
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.