SLC26A4, solute carrier family 26 member 4, 5172

N. diseases: 194; N. variants: 174
Disease: hearing impairment ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1554362735
rs1554362735
Entrez Id: 5172
Gene Symbol: SLC26A4
SLC26A4
CUI: C1384666
Disease:
hearing impairment 		AGCTGG 0.700 CausalMutation CLINVAR