CLRN2 - Gene browser | 3billion

CLRN2

CLRN2

clarin 2

HCNC Approved Symbol: CLRN2 (HGNC:33939)
Genomic Coordinates: 4:17,515,165 - 17,527,104 (4p15.32)
Synonyms: DFNB117
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

2Patients

In total, 2 patients were diagnosed with a variant in the CLRN2 gene.

Frequently observed phenotypes(Top 5 only)

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

02
Patient count

Hearing impairment: 2 (100.0%)
Patient Count: 2 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (100.0%)
Hearing loss: 1 (50.0%)
Patient Count: 1 (50.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (50.0%)
Tinnitus: 1 (50.0%)
Patient Count: 1 (50.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (50.0%)

Last updated: 2024-06-30

CLRN2 - Gene browser | 3billion