Gene entry
MYOM1
myomesin 1
- Chromosome
- 18
- Cytoband
- 18p11.31
- Variants (rsID)
- 65
MYOM1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 18 (region 18p11.31). Its official name is “myomesin 1”. The reference table lists 65 variants (rsID) for this gene.
Clinically classified variants
23 reference-table entries with clinical significance.
- rs1071600Benignsingle nucleotide variantCardiovascular phenotype|Hypertrophic cardiomyopathy
- rs117342470Benignsingle nucleotide variantHypertrophic cardiomyopathy|Cardiovascular phenotype
- rs139422575Benignsingle nucleotide variantHypertrophic cardiomyopathy|Cardiovascular phenotype
- rs143030509Benignsingle nucleotide variantHypertrophic cardiomyopathy|Cardiovascular phenotype
- rs149528866Benignsingle nucleotide variantHypertrophic cardiomyopathy|Cardiovascular phenotype
- rs188319622Benignsingle nucleotide variantHypertrophic cardiomyopathy
- rs188677538Benignsingle nucleotide variantHypertrophic cardiomyopathy|Cardiovascular phenotype
- rs1962519Benignsingle nucleotide variantCardiovascular phenotype|Hypertrophic cardiomyopathy
- rs3765623Benignsingle nucleotide variantCardiovascular phenotype|Hypertrophic cardiomyopathy
- rs73373171Benignsingle nucleotide variantHypertrophic cardiomyopathy|Cardiovascular phenotype
- rs76382984Benignsingle nucleotide variantHypertrophic cardiomyopathy|Cardiovascular phenotype
- rs77613865Benignsingle nucleotide variantHypertrophic cardiomyopathy|Cardiovascular phenotype
- rs948298Benignsingle nucleotide variantHypertrophic cardiomyopathy
- rs9807556Benignsingle nucleotide variantHypertrophic cardiomyopathy|Cardiovascular phenotype
- rs187108957Likely benignsingle nucleotide variantHypertrophic cardiomyopathy
- rs199900004Likely benignsingle nucleotide variantHypertrophic cardiomyopathy
- rs201544310Likely benignsingle nucleotide variantHypertrophic cardiomyopathy
- rs183139046Uncertain significancesingle nucleotide variantHypertrophic cardiomyopathy
- rs183881662Uncertain significancesingle nucleotide variantArrhythmogenic right ventricular cardiomyopathy|Hypertrophic cardiomyopathy
- rs184774935Uncertain significancesingle nucleotide variantHypertrophic cardiomyopathy
- rs185573271Uncertain significancesingle nucleotide variantHypertrophic cardiomyopathy
- rs190368385Uncertain significancesingle nucleotide variantHypertrophic cardiomyopathy
- rs199520642Uncertain significancesingle nucleotide variantHypertrophic cardiomyopathy
Other listed variants
- rs4441365
- rs4613146
- rs4798064
- rs6506070
- rs7505690
- rs7506674
- rs8084091
- rs8089599
- rs8091028
- rs9951849
- rs9952207
- rs9955283
- rs11081005
- rs11665602
- rs11874398
- rs12605942
- rs12606145
- rs28463942
- rs28575688
- rs34647598
- rs35797027
- rs62074941
- rs62074943
- rs72860214
- rs72861635
- rs73377266
- rs73937185
- rs74744623
- rs74884432
- rs76037241
- rs76092592
- rs76706567
- rs77619381
- rs78192102
- rs78567624
- rs79933577
- rs117849256
- rs138431527
- rs147299197
- rs192079897
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.