SLC5A5, solute carrier family 5 member 5, 6528

N. diseases: 195; N. variants: 8
Disease: Thyroid Dyshormonogenesis 1 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121909175
rs121909175
Entrez Id: 6528
Gene Symbol: SLC5A5
SLC5A5
CUI: C1848805
Disease:
Thyroid Dyshormonogenesis 1 		A 0.700 CausalMutation CLINVAR