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: rs71530923
rs71530923
Entrez Id: 7466
Gene Symbol: WFS1
WFS1
CUI: C4551693
Disease:
Wolfram Syndrome 1 		T 0.700 CausalMutation CLINVAR Replication of the association between variants in WFS1 and risk of type 2 diabetes in European populations. 18040659 2008
dbSNP: rs71530923
rs71530923
Entrez Id: 7466
Gene Symbol: WFS1
WFS1
CUI: C4551693
Disease:
Wolfram Syndrome 1 		T 0.700 CausalMutation CLINVAR Common variants in WFS1 confer risk of type 2 diabetes. 17603484 2007
dbSNP: rs71530923
rs71530923
Entrez Id: 7466
Gene Symbol: WFS1
WFS1
CUI: C4551693
Disease:
Wolfram Syndrome 1 		T 0.700 CausalMutation CLINVAR Evidence of an increased risk of hearing loss in heterozygous carriers in a Wolfram syndrome family. 9856492 1998