WFS1, wolframin ER transmembrane glycoprotein, 7466

N. diseases: 185; N. variants: 80
Disease: Wolfram Syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs145639028
rs145639028
Entrez Id: 7466
Gene Symbol: WFS1
WFS1
CUI: C0043207
Disease:
Wolfram Syndrome 		0.010 GeneticVariation BEFREE c.376G>A mutation in WFS1 gene causes Wolfram syndrome without deafness. 26773575 2016