SLC26A3, solute carrier family 26 member 3, 1811

N. diseases: 128; N. variants: 58
Disease: Congenital chloride diarrhea ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs386833480
rs386833480
Entrez Id: 1811
Gene Symbol: SLC26A3
SLC26A3
CUI: C0267662
Disease:
Congenital chloride diarrhea 		A 0.800 GeneticVariation CLINVAR
dbSNP: rs386833480
rs386833480
Entrez Id: 1811
Gene Symbol: SLC26A3
SLC26A3
CUI: C0267662
Disease:
Congenital chloride diarrhea 		0.800 GeneticVariation UNIPROT