KCNH2 - Gene browser

KCNH2

potassium voltage-gated channel subfamily H member 2

HCNC Approved Symbol: KCNH2 (HGNC:6251)
Genomic Coordinates: 7:150,944,961 - 150,978,321 (7q36.1)
Synonyms: Kv11.1, HERG, erg1, LQT2
Disease Associations: This gene is associated with the following 2 diseases in OMIM.

20Patients

In total, 20 patients were diagnosed with a variant in the KCNH2 gene.

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

020
Patient count

Left ventricular hypertrophy: 5 (25.0%)
Patient Count: 5 (25.0%)
% of total patients presenting each phenotype is shown in parentheses.
5 (25.0%)
Prolonged qt interval: 3 (15.0%)
Patient Count: 3 (15.0%)
% of total patients presenting each phenotype is shown in parentheses.
3 (15.0%)
Heart failure: 3 (15.0%)
Patient Count: 3 (15.0%)
% of total patients presenting each phenotype is shown in parentheses.
3 (15.0%)
Arrhythmia: 2 (10.0%)
Patient Count: 2 (10.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (10.0%)
Arrhythmias: 2 (10.0%)
Patient Count: 2 (10.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (10.0%)