Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104893882
rs104893882
WFS1
0.800 GeneticVariation UNIPROT Targeted genomic capture and massively parallel sequencing to identify novel variants causing Chinese hereditary hearing loss. 25388789

2014
dbSNP: rs104893882
rs104893882
WFS1
0.800 GeneticVariation UNIPROT WFS1 and non-syndromic low-frequency sensorineural hearing loss: a novel mutation in a Portuguese case. 24462758

2014
dbSNP: rs104893883
rs104893883
WFS1
0.800 GeneticVariation UNIPROT WFS1 and non-syndromic low-frequency sensorineural hearing loss: a novel mutation in a Portuguese case. 24462758

2014
dbSNP: rs104893883
rs104893883
WFS1
0.800 GeneticVariation UNIPROT Targeted genomic capture and massively parallel sequencing to identify novel variants causing Chinese hereditary hearing loss. 25388789

2014
dbSNP: rs104893882
rs104893882
WFS1
0.800 GeneticVariation UNIPROT Identification of two novel missense WFS1 mutations, H696Y and R703H, in patients with non-syndromic low-frequency sensorineural hearing loss. 21356526

2011
dbSNP: rs104893883
rs104893883
WFS1
0.800 GeneticVariation UNIPROT Identification of two novel missense WFS1 mutations, H696Y and R703H, in patients with non-syndromic low-frequency sensorineural hearing loss. 21356526

2011
dbSNP: rs104893882
rs104893882
WFS1
0.800 GeneticVariation UNIPROT Autoimmune disease in a DFNA6/14/38 family carrying a novel missense mutation in WFS1. 18688868

2008
dbSNP: rs104893882
rs104893882
WFS1
0.800 GeneticVariation UNIPROT A novel WFS1 mutation in a family with dominant low frequency sensorineural hearing loss with normal VEMP and EcochG findings. 18518985

2008
dbSNP: rs104893883
rs104893883
WFS1
0.800 GeneticVariation UNIPROT A novel WFS1 mutation in a family with dominant low frequency sensorineural hearing loss with normal VEMP and EcochG findings. 18518985

2008
dbSNP: rs104893883
rs104893883
WFS1
0.800 GeneticVariation UNIPROT Autoimmune disease in a DFNA6/14/38 family carrying a novel missense mutation in WFS1. 18688868

2008
dbSNP: rs104893882
rs104893882
WFS1
0.800 GeneticVariation UNIPROT A novel mutation in the WFS1 gene identified in a Taiwanese family with low-frequency hearing impairment. 17517145

2007
dbSNP: rs104893883
rs104893883
WFS1
0.800 GeneticVariation UNIPROT A novel mutation in the WFS1 gene identified in a Taiwanese family with low-frequency hearing impairment. 17517145

2007
dbSNP: rs104893882
rs104893882
WFS1
0.800 GeneticVariation UNIPROT Confirmation of genetic homogeneity of nonsyndromic low-frequency sensorineural hearing loss by linkage analysis and a DFNA6/14 mutation in a Japanese family. 12181639

2002
dbSNP: rs104893883
rs104893883
WFS1
0.800 GeneticVariation UNIPROT Confirmation of genetic homogeneity of nonsyndromic low-frequency sensorineural hearing loss by linkage analysis and a DFNA6/14 mutation in a Japanese family. 12181639

2002
dbSNP: rs104893882
rs104893882
WFS1
0.800 GeneticVariation UNIPROT Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss. 11709537

2001
dbSNP: rs104893882
rs104893882
WFS1
0.800 GeneticVariation UNIPROT Non-syndromic progressive hearing loss DFNA38 is caused by heterozygous missense mutation in the Wolfram syndrome gene WFS1. 11709538

2001
dbSNP: rs104893883
rs104893883
WFS1
0.800 GeneticVariation UNIPROT Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss. 11709537

2001
dbSNP: rs104893883
rs104893883
WFS1
0.800 GeneticVariation UNIPROT Non-syndromic progressive hearing loss DFNA38 is caused by heterozygous missense mutation in the Wolfram syndrome gene WFS1. 11709538

2001
dbSNP: rs104893882
rs104893882
WFS1
C 0.800 CausalMutation CLINVAR

dbSNP: rs104893883
rs104893883
WFS1
C 0.800 CausalMutation CLINVAR

dbSNP: rs28937893
rs28937893
WFS1
A 0.800 CausalMutation CLINVAR

dbSNP: rs28937893
rs28937893
WFS1
0.800 GeneticVariation UNIPROT

dbSNP: rs121912618
rs121912618
WFS1
0.700 GeneticVariation UNIPROT WFS1 and non-syndromic low-frequency sensorineural hearing loss: a novel mutation in a Portuguese case. 24462758

2014
dbSNP: rs121912618
rs121912618
WFS1
0.700 GeneticVariation UNIPROT Targeted genomic capture and massively parallel sequencing to identify novel variants causing Chinese hereditary hearing loss. 25388789

2014
dbSNP: rs141328044
rs141328044
WFS1
0.700 GeneticVariation UNIPROT WFS1 and non-syndromic low-frequency sensorineural hearing loss: a novel mutation in a Portuguese case. 24462758

2014