Gene entry
MYOZ2
myozenin 2
- Chromosome
- 4
- Cytoband
- 4q26
- Variants (rsID)
- 14
MYOZ2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 4 (region 4q26). Its official name is “myozenin 2”. The reference table lists 14 variants (rsID) for this gene.
Clinically classified variants
6 reference-table entries with clinical significance.
- rs140126678Benignsingle nucleotide variantHypertrophic cardiomyopathy 16|Hypertrophic cardiomyopathy
- rs146320826Benignsingle nucleotide variant
- rs149125238Benignsingle nucleotide variantHypertrophic cardiomyopathy|Cardiomyopathy
- rs76757102Benignsingle nucleotide variantCardiovascular phenotype|Hypertrophic cardiomyopathy|Hypertrophic cardiomyopathy 16|Hypertrophic cardiomyopathy|Cardiomyopathy|Cardiomyopathy
- rs143345726Conflicting interpretationssingle nucleotide variantCardiovascular phenotype|Hypertrophic cardiomyopathy|Hypertrophic cardiomyopathy 16|Restrictive cardiomyopathy|Cardiomyopathy
- rs372006344Likely benignsingle nucleotide variantHypertrophic cardiomyopathy
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.