TNNC1 - Gene browser

TNNC1

troponin C1, slow skeletal and cardiac type

HCNC Approved Symbol: TNNC1 (HGNC:11943)
Genomic Coordinates: 3:52,451,100 - 52,454,041 (3p21.1)
Synonyms: TNNC
Disease Associations: This gene is associated with the following 2 diseases in OMIM.

12Patients

In total, 12 patients were diagnosed with a variant in the TNNC1 gene.

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

012
Patient count

Left ventricular hypertrophy: 7 (58.3%)
Patient Count: 7 (58.3%)
% of total patients presenting each phenotype is shown in parentheses.
7 (58.3%)
Hypertrophic cardiomyopathy: 3 (25.0%)
Patient Count: 3 (25.0%)
% of total patients presenting each phenotype is shown in parentheses.
3 (25.0%)
Arrhythmias: 3 (25.0%)
Patient Count: 3 (25.0%)
% of total patients presenting each phenotype is shown in parentheses.
3 (25.0%)
Cardiomyopathy: 2 (16.7%)
Patient Count: 2 (16.7%)
% of total patients presenting each phenotype is shown in parentheses.
2 (16.7%)
Arrhythmia: 2 (16.7%)
Patient Count: 2 (16.7%)
% of total patients presenting each phenotype is shown in parentheses.
2 (16.7%)