SLC26A4, solute carrier family 26 member 4, 5172

N. diseases: 194; N. variants: 174
Disease: Sensorineural hearing loss, bilateral ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1554358720
rs1554358720
Entrez Id: 5172
Gene Symbol: SLC26A4
SLC26A4
CUI: C0452138
Disease:
Sensorineural hearing loss, bilateral 		CT 0.700 CausalMutation CLINVAR