SLC26A4, solute carrier family 26 member 4, 5172

N. diseases: 194; N. variants: 174
Disease: Graves Disease ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs111033243
rs111033243
Entrez Id: 5172
Gene Symbol: SLC26A4
SLC26A4
CUI: C0018213
Disease:
Graves Disease 		0.010 GeneticVariation BEFREE The p.F354S variation was identified both among patients (1~HT and 3 GD) and healthy subjects (n=5). 21045265 2010
dbSNP: rs111033304
rs111033304
Entrez Id: 5172
Gene Symbol: SLC26A4
SLC26A4
CUI: C0018213
Disease:
Graves Disease 		0.010 GeneticVariation BEFREE Whereas, the p.I300L variant was identified only in GD patients (n=3). 21045265 2010