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: rs752461187
rs752461187
Entrez Id: 7466
Gene Symbol: WFS1
WFS1
CUI: C4551693
Disease:
Wolfram Syndrome 1 		C 0.700 GeneticVariation CLINVAR Wolfram syndrome in the Japanese population; molecular analysis of WFS1 gene and characterization of clinical features. 25211237 2014