ClinVar Miner

List of variants in gene WFS1 reported as uncertain significance for autosomal dominant nonsyndromic deafness 6

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 18
Download table as spreadsheet
HGVS dbSNP
NM_006005.3(WFS1):c.1079G>A (p.Cys360Tyr) rs147157374
NM_006005.3(WFS1):c.1124G>A (p.Arg375His) rs142671083
NM_006005.3(WFS1):c.1167T>G (p.Asp389Glu) rs201282601
NM_006005.3(WFS1):c.1235T>C (p.Val412Ala) rs144951440
NM_006005.3(WFS1):c.1297G>A (p.Ala433Thr) rs138771366
NM_006005.3(WFS1):c.1371G>T (p.Arg457Ser) rs113446173
NM_006005.3(WFS1):c.1396G>A (p.Gly466Ser) rs727503750
NM_006005.3(WFS1):c.1538A>C (p.Tyr513Ser) rs544933961
NM_006005.3(WFS1):c.1633G>A (p.Val545Met) rs201993978
NM_006005.3(WFS1):c.1724C>G (p.Ala575Gly) rs71524360
NM_006005.3(WFS1):c.1846G>T (p.Ala616Ser) rs553336498
NM_006005.3(WFS1):c.1957C>T (p.Arg653Cys) rs201064551
NM_006005.3(WFS1):c.2029G>A (p.Ala677Thr) rs757027394
NM_006005.3(WFS1):c.535G>A (p.Ala179Thr) rs776685250
NM_006005.3(WFS1):c.683G>A (p.Arg228His) rs150771247
NM_006005.3(WFS1):c.716A>G (p.Lys239Arg) rs727503747
NM_006005.3(WFS1):c.728C>T (p.Ala243Val) rs147147660
NM_006005.3(WFS1):c.817G>A (p.Glu273Lys) rs142428158

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.