Gene entry
MYLK2
myosin light chain kinase 2
- Chromosome
- 20
- Cytoband
- 20q11.21
- Variants (rsID)
- 15
MYLK2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 20 (region 20q11.21). Its official name is “myosin light chain kinase 2”. The reference table lists 15 variants (rsID) for this gene.
Clinically classified variants
12 reference-table entries with clinical significance.
- rs121908108Benignsingle nucleotide variantCardiomyopathy, hypertrophic, midventricular, digenic|Hypertrophic cardiomyopathy 1|Cardiomyopathy
- rs138130914Benignsingle nucleotide variantCardiomyopathy|Hypertrophic cardiomyopathy 1|Hypertrophic cardiomyopathy
- rs17340492Benignsingle nucleotide variantHypertrophic cardiomyopathy 1|Cardiomyopathy
- rs193922713Benignsingle nucleotide variantHypertrophic cardiomyopathy 1
- rs28763880Benignsingle nucleotide variantHypertrophic cardiomyopathy 1|Cardiomyopathy
- rs34396614Benignsingle nucleotide variantCardiomyopathy|Hypertrophic cardiomyopathy 1
- rs369603764Benignsingle nucleotide variantHypertrophic cardiomyopathy 1
- rs6089088Benignsingle nucleotide variantHypertrophic cardiomyopathy 1
- rs117502839Conflicting interpretationssingle nucleotide variantLong QT syndrome|Ventricular tachycardia|Cardiomyopathy|Hypertrophic cardiomyopathy 1|Cardiomyopathy
- rs142620954Conflicting interpretationssingle nucleotide variantHypertrophic cardiomyopathy 1
- rs193922712Conflicting interpretationssingle nucleotide variantCardiomyopathy|Hypertrophic cardiomyopathy 1
- rs779637525Likely benignsingle nucleotide variantHypertrophic cardiomyopathy 1
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.