MYL2 - Gene browser

MYL2

myosin light chain 2

HCNC Approved Symbol: MYL2 (HGNC:7583)
Genomic Coordinates: 12:110,910,845 - 110,921,449 (12q24.11)
Synonyms: CMH10
Disease Associations: This gene is associated with the following 2 diseases in OMIM.

13Patients

In total, 13 patients were diagnosed with a variant in the MYL2 gene.

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

013
Patient count

Left ventricular hypertrophy: 12 (92.3%)
Patient Count: 12 (92.3%)
% of total patients presenting each phenotype is shown in parentheses.
12 (92.3%)
Heart failure: 3 (23.1%)
Patient Count: 3 (23.1%)
% of total patients presenting each phenotype is shown in parentheses.
3 (23.1%)
Arrhythmias: 2 (15.4%)
Patient Count: 2 (15.4%)
% of total patients presenting each phenotype is shown in parentheses.
2 (15.4%)
Hypertrophic cardiomyopathy: 1 (7.7%)
Patient Count: 1 (7.7%)
% of total patients presenting each phenotype is shown in parentheses.
1 (7.7%)
Pain: 1 (7.7%)
Patient Count: 1 (7.7%)
% of total patients presenting each phenotype is shown in parentheses.
1 (7.7%)