RS1 - Gene browser

RS1

retinoschisin 1

HCNC Approved Symbol: RS1 (HGNC:10457)
Genomic Coordinates: 23:18,639,688 - 18,672,108 (Xp22.13)
Synonyms: XLRS1, RS
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

29Patients

In total, 29 patients were diagnosed with a variant in the RS1 gene.

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

029
Patient count

Retinoschisis: 15 (51.7%)
Patient Count: 15 (51.7%)
% of total patients presenting each phenotype is shown in parentheses.
15 (51.7%)
Night blindness: 7 (24.1%)
Patient Count: 7 (24.1%)
% of total patients presenting each phenotype is shown in parentheses.
7 (24.1%)
Decreased visual acuity: 6 (20.7%)
Patient Count: 6 (20.7%)
% of total patients presenting each phenotype is shown in parentheses.
6 (20.7%)
Poor vision: 3 (10.3%)
Patient Count: 3 (10.3%)
% of total patients presenting each phenotype is shown in parentheses.
3 (10.3%)
Retinal dystrophy: 3 (10.3%)
Patient Count: 3 (10.3%)
% of total patients presenting each phenotype is shown in parentheses.
3 (10.3%)