WFS1, wolframin ER transmembrane glycoprotein, 7466

N. diseases: 185; N. variants: 80
Disease: Wolfram Syndrome 1 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1560408865
rs1560408865
Entrez Id: 7466
Gene Symbol: WFS1
WFS1
CUI: C4551693
Disease:
Wolfram Syndrome 1 		G 0.700 CausalMutation CLINVAR Phenotypic characteristics of early Wolfram syndrome. 23981289 2013