Gene entry
MYL3
myosin light chain 3
- Chromosome
- 3
- Cytoband
- 3p21.31
- Variants (rsID)
- 24
MYL3 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 3 (region 3p21.31). Its official name is “myosin light chain 3”. The reference table lists 24 variants (rsID) for this gene.
Clinically classified variants
21 reference-table entries with clinical significance.
- rs2227294Benignsingle nucleotide variantHypertrophic cardiomyopathy 8
- rs104893750Conflicting interpretationssingle nucleotide variantHypertrophic cardiomyopathy 8|Hypertrophic cardiomyopathy|Cardiovascular phenotype|Cardiomyopathy|Primary familial hypertrophic cardiomyopathy
- rs1064793448Conflicting interpretationsDeletionCardiomyopathy|Hypertrophic cardiomyopathy
- rs139794067Conflicting interpretationssingle nucleotide variantHypertrophic cardiomyopathy|Cardiovascular phenotype|Hypertrophic cardiomyopathy 8|Cardiomyopathy
- rs199474705Conflicting interpretationssingle nucleotide variantHypertrophic cardiomyopathy
- rs199474707Conflicting interpretationssingle nucleotide variantIncreased left ventricular wall thickness|Hypertrophic cardiomyopathy|Cardiovascular phenotype|Primary familial hypertrophic cardiomyopathy|Cardiomyopathy|Hypertrophic cardiomyopathy 8
- rs730880962Conflicting interpretationssingle nucleotide variantHypertrophic cardiomyopathy
- rs869025485Conflicting interpretationssingle nucleotide variantPrimary familial hypertrophic cardiomyopathy|Hypertrophic cardiomyopathy
- rs869025486Conflicting interpretationssingle nucleotide variantPrimary familial hypertrophic cardiomyopathy|Hypertrophic cardiomyopathy
- rs567723663Likely pathogenicsingle nucleotide variant
- rs730880162Likely pathogenicsingle nucleotide variantPrimary familial hypertrophic cardiomyopathy
- rs730880960Likely pathogenicsingle nucleotide variant
- rs104893748Pathogenicsingle nucleotide variantHypertrophic cardiomyopathy 8|Hypertrophic cardiomyopathy
- rs199474703Pathogenicsingle nucleotide variantHypertrophic cardiomyopathy 8|Cardiomyopathy|Hypertrophic cardiomyopathy|Primary familial hypertrophic cardiomyopathy
- rs199474706Pathogenicsingle nucleotide variantHypertrophic cardiomyopathy
- rs104893749Uncertain significancesingle nucleotide variantHypertrophic cardiomyopathy 8|Cardiovascular phenotype|Cardiomyopathy, familial restrictive, 1|Hypertrophic cardiomyopathy|Cardiomyopathy
- rs143852164Uncertain significancesingle nucleotide variantPrimary familial hypertrophic cardiomyopathy|Hypertrophic cardiomyopathy|Cardiovascular phenotype|Cardiomyopathy
- rs150634297Uncertain significancesingle nucleotide variantPrimary familial hypertrophic cardiomyopathy|Hypertrophic cardiomyopathy|Cardiomyopathy
- rs193922391Uncertain significancesingle nucleotide variantPrimary familial hypertrophic cardiomyopathy|Hypertrophic cardiomyopathy|Cardiovascular phenotype|Cardiomyopathy
- rs199474708Uncertain significancesingle nucleotide variantCardiomyopathy|Hypertrophic cardiomyopathy
- rs730880955Uncertain significancesingle nucleotide variant
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.