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: rs797045076
rs797045076
Entrez Id: 7466;107986257
Gene Symbol: WFS1;LOC107986257
WFS1;LOC107986257
CUI: C4551693
Disease:
Wolfram Syndrome 1 		T 0.700 CausalMutation CLINVAR Molecular diagnostic experience of whole-exome sequencing in adult patients. 26633545 2016