WFS1, wolframin ER transmembrane glycoprotein, 7466

N. diseases: 185; N. variants: 80
Disease: Wolfram-Like Syndrome, Autosomal Dominant ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs71539673
rs71539673
Entrez Id: 7466
Gene Symbol: WFS1
WFS1
CUI: C3280358
Disease:
Wolfram-Like Syndrome, Autosomal Dominant 		0.710 GeneticVariation BEFREE The mutation p.(Glu809Lys) in the WFS1 gene is associated with WFSL. 27217304 2016
dbSNP: rs71539673
rs71539673
Entrez Id: 7466
Gene Symbol: WFS1
WFS1
CUI: C3280358
Disease:
Wolfram-Like Syndrome, Autosomal Dominant 		A 0.710 CausalMutation CLINVAR