SLC26A3 - Gene browser

SLC26A3

solute carrier family 26 member 3

HCNC Approved Symbol: SLC26A3 (HGNC:3018)
Genomic Coordinates: 7:107,765,469 - 107,803,223 (7q22.3-q31.1)
Synonyms: DRA, CLD
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

11Patients

In total, 11 patients were diagnosed with a variant in the SLC26A3 gene.

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

011
Patient count

Chronic diarrhea: 7 (63.6%)
Patient Count: 7 (63.6%)
% of total patients presenting each phenotype is shown in parentheses.
7 (63.6%)
Polyhydramnios: 6 (54.5%)
Patient Count: 6 (54.5%)
% of total patients presenting each phenotype is shown in parentheses.
6 (54.5%)
Failure to thrive: 5 (45.5%)
Patient Count: 5 (45.5%)
% of total patients presenting each phenotype is shown in parentheses.
5 (45.5%)
Hyponatremia: 5 (45.5%)
Patient Count: 5 (45.5%)
% of total patients presenting each phenotype is shown in parentheses.
5 (45.5%)
Hypochloremia: 4 (36.4%)
Patient Count: 4 (36.4%)
% of total patients presenting each phenotype is shown in parentheses.
4 (36.4%)