WFS1, wolframin ER transmembrane glycoprotein, 7466

N. diseases: 185; N. variants: 80
Disease: DEAFNESS, AUTOSOMAL DOMINANT 6 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1323852277
rs1323852277
Entrez Id: 7466
Gene Symbol: WFS1
WFS1
CUI: C1833021
Disease:
DEAFNESS, AUTOSOMAL DOMINANT 6 		0.700 GeneticVariation UNIPROT