G WFS1 | |||
Description: wolframin ER transmembrane glycoprotein Associations 88 Studies 79 |
P Variants in WFS1 and Other Mendelian Deafness Genes Are Associated with Cisplatin-Associated Ototoxicity. | |||
Wheeler HE et al. 2016 Clin Cancer Res PMID:28039263 Associations 20 Studies 1 |
V rs1801214 | |||
Location: 4:6301295 Cytogenetic region:4p16.1 Most severe consequence: Missense variant Mapped gene(s): WFS1 Associations 16 Studies 15 |
V rs4458523 | |||
Location: 4:6288259 Cytogenetic region:4p16.1 Most severe consequence: Intron variant Mapped gene(s): WFS1 Associations 2 Studies 2 |
V rs62283056 | |||
Location: 4:6274903 Cytogenetic region:4p16.1 Most severe consequence: Intron variant Mapped gene(s): WFS1 Associations 1 Studies 1 |
V rs1801212 | |||
Location: 4:6300792 Cytogenetic region:4p16.1 Most severe consequence: Missense variant Mapped gene(s): WFS1 Associations 15 Studies 15 |
V rs1046319 | |||
Location: 4:6302559 Cytogenetic region:4p16.1 Most severe consequence: 3 prime utr variant Mapped gene(s): WFS1 Associations 1 Studies 1 |
V rs10755148 | |||
Location: 4:6293337 Cytogenetic region:4p16.1 Most severe consequence: Intron variant Mapped gene(s): WFS1 Associations 2 Studies 2 |
V rs147834269 | |||
Location: 4:6302004 Cytogenetic region:4p16.1 Most severe consequence: Missense variant Mapped gene(s): WFS1 Associations 5 Studies 5 |
V rs12642481 | |||
Location: 4:6299331 Cytogenetic region:4p16.1 Most severe consequence: Intron variant Mapped gene(s): WFS1 Associations 1 Studies 1 |
V rs9997824 | |||
Location: 4:6281526 Cytogenetic region:4p16.1 Most severe consequence: Intron variant Mapped gene(s): WFS1 Associations 1 Studies 1 |
V rs734312 | |||
Location: 4:6301627 Cytogenetic region:4p16.1 Most severe consequence: Missense variant Mapped gene(s): WFS1 Associations 2 Studies 2 |
V rs1046316 | |||
Location: 4:6302360 Cytogenetic region:4p16.1 Most severe consequence: Synonymous variant Mapped gene(s): WFS1 Associations 3 Studies 3 |
V rs111064828 | |||
Location: 4:6299732 Cytogenetic region:4p16.1 Most severe consequence: Intron variant Mapped gene(s): WFS1 Associations 1 Studies 1 |
V rs4689394 | |||
Location: 4:6289276 Cytogenetic region:4p16.1 Most severe consequence: Intron variant Mapped gene(s): WFS1 Associations 1 Studies 1 |
V rs4996963 | |||
Location: 4:6274399 Cytogenetic region:4p16.1 Most severe consequence: Intron variant Mapped gene(s): WFS1 Associations 1 Studies 1 |
V rs9998835 | |||
Location: 4:6291510 Cytogenetic region:4p16.1 Most severe consequence: Intron variant Mapped gene(s): WFS1 Associations 4 Studies 4 |
V rs4688988 | |||
Location: 4:6285729 Cytogenetic region:4p16.1 Most severe consequence: Intron variant Mapped gene(s): WFS1 Associations 1 Studies 1 |
V rs10010131 | |||
Location: 4:6291188 Cytogenetic region:4p16.1 Most severe consequence: Splice polypyrimidine tract variant Mapped gene(s): WFS1 Associations 2 Studies 2 |
V rs4234731 | |||
Location: 4:6298187 Cytogenetic region:4p16.1 Most severe consequence: Intron variant Mapped gene(s): WFS1 Associations 6 Studies 6 |
V rs4688989 | |||
Location: 4:6288867 Cytogenetic region:4p16.1 Most severe consequence: Intron variant Mapped gene(s): WFS1 Associations 2 Studies 2 |
V rs9457 | |||
Location: 4:6303072 Cytogenetic region:4p16.1 Most severe consequence: 3 prime utr variant Mapped gene(s): WFS1 Associations 3 Studies 3 |
V rs12508672 | |||
Location: 4:6286238 Cytogenetic region:4p16.1 Most severe consequence: Intron variant Mapped gene(s): WFS1 Associations 2 Studies 2 |
V rs9998519 | |||
Location: 4:6291182 Cytogenetic region:4p16.1 Most severe consequence: Splice polypyrimidine tract variant Mapped gene(s): WFS1 Associations 1 Studies 1 |
V rs13130845 | |||
Location: 4:6295919 Cytogenetic region:4p16.1 Most severe consequence: Intron variant Mapped gene(s): WFS1 Associations 1 Studies 1 |
V rs4234733 | |||
Location: 4:6314654 Cytogenetic region:4p16.1 Most severe consequence: Intergenic variant Mapped gene(s): WFS1,PPP2R2C Associations 1 Studies 1 |
V rs10937721 | |||
Location: 4:6305036 Cytogenetic region:4p16.1 Most severe consequence: Intergenic variant Mapped gene(s): WFS1,PPP2R2C Associations 4 Studies 4 |
V rs4688992 | |||
Location: 4:6315193 Cytogenetic region:4p16.1 Most severe consequence: Intergenic variant Mapped gene(s): WFS1,PPP2R2C Associations 1 Studies 1 |
V rs7680206 | |||
Location: 4:6318139 Cytogenetic region:4p16.1 Most severe consequence: Intergenic variant Mapped gene(s): WFS1,PPP2R2C Associations 1 Studies 1 |
V rs4689388 | |||
Location: 4:6268329 Cytogenetic region:4p16.1 Most severe consequence: Intergenic variant Mapped gene(s): WFS1,JAKMIP1-DT Associations 7 Studies 6 |