ClinVar Miner

List of variants in gene WFS1 reported as uncertain significance for auditory system disease

Included ClinVar conditions (549):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 121
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HGVS dbSNP
NM_006005.3(WFS1):c.*11C>G
NM_006005.3(WFS1):c.*14C>T
NM_006005.3(WFS1):c.*158G>A
NM_006005.3(WFS1):c.*223C>G
NM_006005.3(WFS1):c.*258A>G rs886059533
NM_006005.3(WFS1):c.*260G>C
NM_006005.3(WFS1):c.*300A>G
NM_006005.3(WFS1):c.*37C>A
NM_006005.3(WFS1):c.*448A>T
NM_006005.3(WFS1):c.*455A>G
NM_006005.3(WFS1):c.*506C>T rs886059536
NM_006005.3(WFS1):c.*520G>A rs573433508
NM_006005.3(WFS1):c.*526A>C rs886059537
NM_006005.3(WFS1):c.*553G>A
NM_006005.3(WFS1):c.*605T>C rs886059538
NM_006005.3(WFS1):c.*654G>A rs886059539
NM_006005.3(WFS1):c.*656C>T
NM_006005.3(WFS1):c.*700C>A rs528424908
NM_006005.3(WFS1):c.-100C>G rs886059524
NM_006005.3(WFS1):c.-105T>G rs886059523
NM_006005.3(WFS1):c.-106A>G rs868329184
NM_006005.3(WFS1):c.-129A>G rs886059522
NM_006005.3(WFS1):c.-130C>T rs576284630
NM_006005.3(WFS1):c.-133G>T rs886059521
NM_006005.3(WFS1):c.-43G>C
NM_006005.3(WFS1):c.-55C>G rs886059525
NM_006005.3(WFS1):c.-93G>C
NM_006005.3(WFS1):c.1024G>A (p.Ala342Thr) rs148028521
NM_006005.3(WFS1):c.1079G>A (p.Cys360Tyr) rs147157374
NM_006005.3(WFS1):c.1099G>A (p.Asp367Asn) rs886059528
NM_006005.3(WFS1):c.1124G>A (p.Arg375His) rs142671083
NM_006005.3(WFS1):c.1134C>G (p.Thr378=) rs71530904
NM_006005.3(WFS1):c.1147C>T (p.Arg383Cys)
NM_006005.3(WFS1):c.115G>A (p.Glu39Lys) rs774330485
NM_006005.3(WFS1):c.1167T>G (p.Asp389Glu) rs201282601
NM_006005.3(WFS1):c.1180G>A (p.Glu394Lys)
NM_006005.3(WFS1):c.1235T>C (p.Val412Ala) rs144951440
NM_006005.3(WFS1):c.1263C>T (p.Ile421=) rs748103155
NM_006005.3(WFS1):c.1265C>T (p.Ala422Val) rs150368988
NM_006005.3(WFS1):c.1297G>A (p.Ala433Thr) rs138771366
NM_006005.3(WFS1):c.1311C>T (p.Gly437=) rs886059529
NM_006005.3(WFS1):c.132C>T (p.Pro44=) rs754346893
NM_006005.3(WFS1):c.1333C>G (p.Leu445Val) rs764932308
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.1399C>T (p.Leu467=) rs142700542
NM_006005.3(WFS1):c.1507G>A (p.Val503Ile) rs573775230
NM_006005.3(WFS1):c.1509C>T (p.Val503=)
NM_006005.3(WFS1):c.1538A>C (p.Tyr513Ser) rs544933961
NM_006005.3(WFS1):c.1580C>T (p.Thr527Ile)
NM_006005.3(WFS1):c.1597C>T (p.Pro533Ser) rs146132083
NM_006005.3(WFS1):c.1633G>A (p.Val545Met) rs201993978
NM_006005.3(WFS1):c.1656C>T (p.Thr552=) rs141477172
NM_006005.3(WFS1):c.168C>T (p.Asp56=) rs112598170
NM_006005.3(WFS1):c.1724C>G (p.Ala575Gly) rs71524360
NM_006005.3(WFS1):c.1739T>A (p.Val580Glu)
NM_006005.3(WFS1):c.176C>T (p.Ala59Val)
NM_006005.3(WFS1):c.1799C>T (p.Thr600Ile) rs886059530
NM_006005.3(WFS1):c.1831C>T (p.Arg611Cys)
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.1969A>G (p.Met657Val) rs71532861
NM_006005.3(WFS1):c.1986C>T (p.Ser662=)
NM_006005.3(WFS1):c.1993A>C (p.Thr665Pro) rs369656458
NM_006005.3(WFS1):c.2011G>T (p.Ala671Ser)
NM_006005.3(WFS1):c.2026C>T (p.Arg676Cys) rs201623184
NM_006005.3(WFS1):c.2029G>A (p.Ala677Thr) rs757027394
NM_006005.3(WFS1):c.2030C>T (p.Ala677Val)
NM_006005.3(WFS1):c.2119G>A (p.Val707Ile) rs71524377
NM_006005.3(WFS1):c.2129C>G (p.Thr710Ser)
NM_006005.3(WFS1):c.2135T>C (p.Ile712Thr)
NM_006005.3(WFS1):c.2138A>G (p.Asp713Gly) rs143280847
NM_006005.3(WFS1):c.2157C>T (p.Ala719=) rs766900991
NM_006005.3(WFS1):c.2191A>G (p.Met731Val) rs144010362
NM_006005.3(WFS1):c.2208C>T (p.Gly736=) rs141020933
NM_006005.3(WFS1):c.2209G>A (p.Glu737Lys) rs147834269
NM_006005.3(WFS1):c.2225G>A (p.Cys742Tyr)
NM_006005.3(WFS1):c.2246C>T (p.Thr749Met)
NM_006005.3(WFS1):c.2285A>G (p.Lys762Arg) rs876658119
NM_006005.3(WFS1):c.2298C>A (p.His766Gln) rs755328574
NM_006005.3(WFS1):c.232G>A (p.Gly78Arg)
NM_006005.3(WFS1):c.2340C>A (p.Gly780=) rs886059531
NM_006005.3(WFS1):c.2347T>C (p.Phe783Leu) rs71526461
NM_006005.3(WFS1):c.2356G>T (p.Gly786Cys)
NM_006005.3(WFS1):c.2371C>T (p.Arg791Cys)
NM_006005.3(WFS1):c.2372G>A (p.Arg791His) rs775659531
NM_006005.3(WFS1):c.2405T>C (p.Ile802Thr)
NM_006005.3(WFS1):c.2424C>T (p.Ser808=) rs56035336
NM_006005.3(WFS1):c.2436C>T (p.Ser812=) rs142630687
NM_006005.3(WFS1):c.2437G>A (p.Val813Met) rs756972444
NM_006005.3(WFS1):c.2453G>A (p.Arg818His) rs575851859
NM_006005.3(WFS1):c.2454C>T (p.Arg818=) rs139223980
NM_006005.3(WFS1):c.2459G>A (p.Gly820Asp) rs764842865
NM_006005.3(WFS1):c.2466C>T (p.Leu822=) rs141669724
NM_006005.3(WFS1):c.2481C>T (p.Thr827=) rs886059532
NM_006005.3(WFS1):c.2498T>A (p.Leu833Gln)
NM_006005.3(WFS1):c.2514T>C (p.Pro838=)
NM_006005.3(WFS1):c.2576G>A (p.Arg859Gln) rs121912618
NM_006005.3(WFS1):c.2580C>T (p.His860=) rs754802246
NM_006005.3(WFS1):c.2595C>A (p.His865Gln) rs142469572
NM_006005.3(WFS1):c.2603G>A (p.Arg868His) rs56393026
NM_006005.3(WFS1):c.2664G>A (p.Ser888=)
NM_006005.3(WFS1):c.2667G>A (p.Ala889=) rs71526454
NM_006005.3(WFS1):c.28C>T (p.Pro10Ser) rs760256649
NM_006005.3(WFS1):c.345C>T (p.Gly115=) rs200385504
NM_006005.3(WFS1):c.400G>A (p.Ala134Thr) rs147724970
NM_006005.3(WFS1):c.445T>C (p.Leu149=)
NM_006005.3(WFS1):c.504C>T (p.Ser168=)
NM_006005.3(WFS1):c.535G>A (p.Ala179Thr) rs776685250
NM_006005.3(WFS1):c.578dup (p.Gln194fs)
NM_006005.3(WFS1):c.654C>T (p.Pro218=) rs727504666
NM_006005.3(WFS1):c.683G>A (p.Arg228His) rs150771247
NM_006005.3(WFS1):c.70C>T (p.Arg24Cys) rs756667462
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.804C>T (p.Asp268=)
NM_006005.3(WFS1):c.817G>A (p.Glu273Lys) rs142428158
NM_006005.3(WFS1):c.81C>T (p.Leu27=)
NM_006005.3(WFS1):c.837T>C (p.Pro279=)
NM_006005.3(WFS1):c.872A>G (p.Tyr291Cys)
NM_006005.3(WFS1):c.95C>T (p.Ser32Leu) rs727504730

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